Disorder of Maxillary and Mandibular Dental Arch RelationshipDD-TENSNCT05096624
Impact of Complete Removable Prosthetic Rehabilitations Performed by an Innovative DDTENS Protocol, on the Quality of Masticatory Function and the Management of Completely Edentulous Patients
A study testing DD-TENS system, Gold Standard and Digital Denture system in people with Disorder of Maxillary and Mandibular Dental Arch Relationship, run by University Hospital, Montpellier at 1 site in France.
Trial summary
Total edentulism is a profound physical, psychic and social handicap, which affects 5 million people in France. The most frequent complaint of edentulous patients rehabilitated by conventional Complete Removable Prostheses (CRP) is the reduction of masticatory efficiency. Read more about this study
- Who is it for?
- Ages 60 to 85 yearsHealthy volunteers can take part
- Conditions the study is for
- Disorder of Maxillary and Mandibular Dental Arch Relationship
- What is being tested?
- DD-TENS system, Gold Standard and Digital Denture system
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteFrance
- Study dates
- 25 Feb 2022to Aug 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 to 85 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Bimaxillary edentulous patients
- Former bimaxillary CRP wearers (transitional or usage)
- Acceptance of the confiscation of the old prosthesis when the new prosthesis is placed in the mouth and during the 4 months the new prosthesis is worn.
- Signed informed consent
Who cannot join
- Dependent patients (under guardianship or patients in EHPAD)
- Heavy pathologies
- Salivary pathologies (Gougerot-Sjögren syndrome) or asialia related to a medication.
- Patients with a pacemaker
- Skeletal class III with an anteroposterior shift of more than 1 cm
- Patients under court protection
Trial locations and contacts
1 site in 1 country.
France1 site, 1 recruiting
- Recruiting
CHU de Montpellier
Montpellier, 34295
Delphine CARAYON, d-carayon@chu-montpellier.fr
Delphine CARAYON
About this study
Total edentulism is a profound physical, psychic and social handicap, which affects 5 million people in France. The most frequent complaint of edentulous patients rehabilitated by conventional Complete Removable Prostheses (CRP) is the reduction of masticatory efficiency. This alteration has medical repercussions and a negative psychological and social impact.
Our study aims to evaluate the impact of an innovative protocol on the quality of masticatory function, prosthetic treatment and, in fact, on the quality of life of the totally edentulous patient. This protocol combines the Digital Denture system with the transcutaneous electrical neurostimulation system (TENS®), in order to improve the balance of the dento-dental contacts of CRP. This new protocol is called DDTENS.
Read more
The first objective of the study is to compare the activity and balance of the masticatory muscles at 1 month (T1) of wearing the prostheses, between an experimental group benefiting from a CRP by the DDTENS protocol and 2 reference groups ( the first benefiting from a CRP by the conventional procedure and the second by the Digital Denture procedure) in bimaxillary total edentulous patients
The secondary objectives are:
- to compare the number of sessions required to obtain a finalized bimaxillary total removable prosthesis between the 3 groups.
- to compare the quality of life of patients with their CRP between the 3 groups, at 1 month and 4 months of wearing the prostheses.
- to compare the activity and balance of the masticatory muscles when the prostheses were put in the mouth (T0) and at 4 months (T4) of wearing the prostheses
The study design is a randomised open-label controlled pilot study with blinded reviewer assessment comparing 3 parallel groups:
- Experimental group: 10 bimaxillary edentulous patients rehabilitated by CRP using the DDTENS protocol.
- Control group 1: 10 edentulous bimaxillary patients rehabilitated by CRP according to the conventional method (gold standard technique).
- Control group 2: 10 edentulous bimaxillary patients rehabilitated by CRP using the Digital Denture procedure.
The expected benefits for patients in the DDTENS experimental group are the optimization of occlusal balance, the optimization of the time of integration of the prosthesis in the mouth, the time saving in the prosthetic treatment of the edentulous patient and the improvement of eating behaviours and quality of life of edentulous patients which would delay the entry of our patients into the sphere of dependence.
These results would allow the validation of a new rehabilitation protocol for the edentulous patient, leading to a modification of clinical practices.
Read the detailed description
EPIDEMIOLOGY Total edentulism is defined by the total absence of teeth. It can be uni or bimaxillary and represents a profound physical, psychic and social handicap, affecting 5 million people in France. Despite progress in prophylaxis, the number of patients with total edentulism is constantly increasing.
There are several explanations for this phenomenon in France:
- Increase in life expectancy According to INSEE, life expectancy in France will increase from 75.2 years to 89.5 years for men and from 82.7 to 93 years for women between 2000 and 2050.
- Social precarity Social precarity is a societal problem that explains the delay or lack of dental care, leading to a higher rate of total edentulism among the most disadvantaged social class populations. Lifestyle behaviors such as smoking and alcohol consumption worsen this situation.
- Ageing of the population The arrival of the baby boomers in the 60+ age group and the increase in life expectancy explain the inevitable ageing of the population (3). People aged over 60 are expected to represent 1/3 of the population in 2050, whereas in 2005 they represented only 1/5.
This ageing is often associated with an alteration in physical and intellectual faculties. The relative well-being of 60-75 year old is gradually giving way to frailty. The challenge is to care for increasingly elderly edentulous patients. It is therefore essential to develop prosthetic rehabilitation practices to improve patient comfort.
Adopting an adapted treatment by limiting the number of appointments while maintaining an optimal quality of care is one of the objectives of our project.
PROBLEMATIC OF TOTAL EDENTULISM In the totally edentulous patient, certain physiological functions are altered (mastication, swallowing, taste, phonation). The most frequent complaint of edentulous patients rehabilitated by conventional Complete Removable Prosthesis (CRP) is the decrease in masticatory capacity. The masticatory capacity of edentulous patients is equivalent to 1/6 of dentate patients, not to mention the changes in eating behavior with certain foods banned from daily life.
This observation has medical repercussions (nutritional deficiencies, change in eating behavior, risk of misdirection, etc.) and a harmful psychological and social impact.
STATUS OF THE ISSUE Chewing ability can be understood by the shape of the chewing cycle, by bite force or by chewing efficiency. Studies have confirmed that conventional CRP do not restore optimal and efficient masticatory function, due to a lack of precision in the fabrication of the prosthesis and the empirical phase of occlusal balancing. Indeed, the dento-dental contacts, governed by the prosthetic mounting of the teeth, have a major impact on the functioning of the manducatory system.
These functional deficiencies can lead to a loss of physical and psychological autonomy, the gateway to iatrogenic dependence of the elderly in our hospitals.
How to improve masticatory efficiency in the totally edentulous patient? The placement of implants can be an alternative to remedy the problem of CRP retention, but the implant solution is not always feasible.
How to improve masticatory efficiency in the totally edentulous patient without the help of implants? The prosthetic equilibrium of an osteo-muco-portal prosthesis without implants is intimately linked to the tissue equilibrium and the neuro-musculo-articular equilibrium. Conversely, an unstable prosthesis leads to tissue damage and joint disorders.
The stability of the prosthesis is linked to the occlusal balance, the balance of the dento-dental contacts between the two arches. The complexity of the treatment lies in the determination of the inter-arch relationship or maxillo-mandibular relationship (MMR), in the vertical and horizontal directions. Indeed, in the totally edentulous patient, we have no reference points. The only usable determinants are the temporomandibular joints (TMJ).
To date, the conventional therapy or gold standard technique used for the rehabilitation of the totally edentulous patient, consists in recreating a "prosthetic substitution normality" by recording the maxillo-mandibular relationship, by putting the mandible in a reproducible position: the position of centered relation. The definition of the National College of Occlusodontics in 2001 tells us that it corresponds "to the condylar reference situation corresponding to a high, simultaneous condylo-disco-temporal coaptation obtained by non forced control. It is reproducible in a given time and for a given body posture and recordable from a mandibular rotation movement". The problem is that the TMJ is rarely healthy resulting in a more or less empirical and operator-dependent mandibular position. Errors in recording the mandibular position result in a loss of accuracy and an increased number of adjustment sessions.
In 2020, the use of digital tools aims to optimize and improve the recording of useful clinical data, the design and manufacture of a sustainable CRP. At present, no consensus exists but 2 paradigms coexist: the partial use of the digital tool, which punctuates the conventional steps and the use of protocols built entirely around the digital tool. These protocols have emerged secondarily and propose complete systems in 2 or 4 sessions.
Computer Aided Design and Manufacturing (CADCAM) systems applied to the rehabilitation of the totally edentulous patient are called Digital Denture protocols. Although CAD/CAM is a digital tool that has been used for many years in dentistry for the dentate patient, the Digital Denture system is not very widespread at the moment. This system ensures a better adaptation of the complete removable prostheses, thanks to the type of manufacture of the prostheses by machining, and a saving of time during the realization of the prostheses.
All in all, there is still the problem of the precision of the recording of the maxillo-mandibular relationship, which can lead to a number of additional adjustment sessions.
From these clinical findings, the two issues of this project were born:
- How to improve the registration of the maxillomandibular relationship and the accuracy of occlusal balance?
- How to reduce the number of adjustment sessions? Ultimately, the answer to these problems would influence the quality of the masticatory function and consequently the quality of life of the totally edentulous person.
INNOVATION The idea of the DDTENS protocol came from the reflection on the dentate patient with cranio-mandibular dysfunctions. Indeed, a transcutaneous electrical neurostimulation system (TENS®) is used in this clinical case, which allows muscular relaxation and the optimization of dento-dental contacts and thus the rebalancing of bilateral muscular forces.
The innovation consists in setting up an innovative protocol combining 2 existing systems: the Digital Denture system and a neuromuscular and electromyographic approach, via the transcutaneous electrical neurostimulation system (TENS®), in order to improve the registration and balance of dento-dental contacts in CRP.
HYPOTHESIS
- Non-operator depending on the maxillo-mandibular relationship recording with a neuro-musculo-articular reference.
- Reduction in the number of sessions for adjusting the prosthesis.
- Optimization of the prosthetic treatment of edentulous patients.
- Improvement of the occlusal balance and therefore of the quality of the masticatory function of edentulous patients (improvement of mastication, of eating behaviors (impact on nutrition, digestion, etc.), making it possible to delay the entry of our patients into the sphere of dependence.
OBJECTIVES
- Compare, within the framework of a randomized controlled pilot study, the activity and balance of the masticatory muscles at 1 month (T1) of wearing the prostheses, measured by a digital system combining electronic recording of mandibular movements and surface electromyography (K7 Evaluation System®), between an experimental group benefiting from a CRP by the DDTENS protocol and 2 reference groups: the first group benefiting from the performance of a CRP by the conventional procedure and the second by the Digital Denture procedure, in bimaxillary total edentulous patients
- Compare between the 3 groups, the number of sessions necessary to obtain a finalized prosthesis (prostheses are considered finalized when the prostheses worn by the patient are occlusally balanced and do not cause any mucosal injury).
- Compare the quality of life of patients with their PRC (assessment of chewing power, eating behavior, etc.), between the 3 groups, at 1 month and 4 months of wearing the prostheses.
- Compare, between the 3 groups, the activity and balance of the masticatory muscles when the prostheses are put in the mouth (T0) and at 4 months (T4) of wearing the prostheses.
METHODOLOGY The study design is a randomised, open-label, controlled pilot study with blinded reviewer evaluation comparing 3 parallel groups (2 control group and 1 experimental group).
The number of subjects to be included is 30. The randomization will be centralized (Ennov clinical software) and stratified by minimization on sex and age (60-69 and 70-85 years).
The masticatory muscle activity and balance are measured by a digital system combining electronic recording of mandibular movements and surface electromyography system (K7 Evaluation System®)
- Measurement of muscle activity = measurements will be made for all muscles at rest with and without prostheses.
- Muscle balance analysis = comparison of right and left muscle activity.
- Analysis of the chronology of muscle contraction on the right and left = muscle contraction symmetry
The number of sessions required to obtain a finished prosthesis recorded for each patient is listed.
The quality of life of the patients is assessed using a specific oral health measurement questionnaire (GOHAI). The GOHAI includes 12 items with 3 sub-dimensions (functional, psycho-social and pain/discomfort).
For each assessment (inclusion visit, 1-month post completion visit and 4-month post completion visit), the 3 sub-dimensions will be analyzed.
The patient must answer the 12 questions with "Never", "Rarely", "Sometimes", "Often" or "Always" (only one answer possible). Each answer is scored from 5 to 1 in this order, except for questions 3, 5 and 7 where the values are reversed. The associated total score varies from 12 to 60. The higher the score, the better the oral quality of life. The score obtained is classified into three categories:
12< <50: poor oral quality of life 51< <56: average oral quality of life 57< <60: good oral quality of life
ANTICIPATED BENEFITS AND RISKS
The expected benefits for patients in the TENS experimental group are:
- Optimization of maxillomandibular relationship registration
- Optimization of occlusal balance and masticatory functions (dental and muscular)
- Optimization of the integration time of prostheses in the mouth
- Improvement of the eating behaviors and quality of life of edentulous patients
- Time saving in the prosthetic treatment of the edentulous patient
The expected risks are:
- Muscle fatigue during TENS sessions if the application time is longer than 60 minutes.
- Number of adjustment sessions equivalent to the current Digital Denture protocol.
EXPECTED RESULTS AND PERSPECTIVES These results would allow the validation of a new gold standard protocol for the rehabilitation of the edentulous patient, leading to a modification of clinical practices.
Perspectives : This study could serve as the basis for an inter-CHU multicenter study as well as the creation and provision of a database (cohort) for artificial intelligence procedures.
- Being tested
- DD-TENS system, Gold Standard, Digital Denture system
- Keywords
- Total bimaxillary edentulous patient, Digital Denture, Neuromuscular occlusion
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DD-TENS systemOther
Use of DD-TENS system
Gold StandardOther
Gold standard
Digital Denture systemOther
Use of Digital Denture system
| Study group | Role | What they receive |
|---|---|---|
| DD-TENS (Digital Denture-Transcutaneous Electrical Nerve Stimulation) | Experimental | Patient with Complete Removable Prostheses according to DD-TENS system Receives: Other: DD-TENS system |
| Gold standard | Active comparator | Patient with Complete Removable Prostheses according to usual care Receives: Other: Gold Standard |
| Digital denture System | Active comparator | Patient with Complete Removable Prostheses according to Digital Denture system Receives: Other: Digital Denture system |
What is being measured
The primary outcome is the main question the study is designed to answer.
masticatory muscle activity at 1 month of wearing prostheses
Measurement of muscle activity = measurements will be made for all muscles at rest with and without prostheses.
Measured: 1month
masticatory muscle balance at 1 month of wearing prostheses
Muscle balance analysis = comparison of right and left muscle activity.
Measured: 1month
Secondary outcomes (8)
number of sessions required to obtain a finalized prosthesis
The number of sessions required to obtain a finalized prosthesis recorded for each patient is listed.
Measured: 1 month
quality of life of the patients at 1 month of wearing the prosthesis
The quality of life of the patients is assessed using a specific oral health measurement questionnaire (GOHAI). The GOHAI includes 12 items with 3 sub-dimensions (functional, psycho-social and pain/discomfort).
For each assessment (inclusion visit, 1-month post completion visit and 4-month post completion visit), the 3 sub-dimensions will be analyzed.
The patient must answer the 12 questions with "Never", "Rarely", "Sometimes", "Often" or "Always" (only one answer possible). Each answer is scored from 5 to 1 in this order, except for questions 3, 5 and 7 where the values are reversed. The associated total score varies from 12 to 60. The higher the score, the better the oral quality of life. The score obtained is classified into three categories:
12< <50: poor oral quality of life 51< <56: average oral quality of life 57< <60: good oral quality of life
Measured: 1 month
quality of life of the patients at 4 months of wearing the prosthesis
The quality of life of the patients is assessed using a specific oral health measurement questionnaire (GOHAI). The GOHAI includes 12 items with 3 sub-dimensions (functional, psycho-social and pain/discomfort).
For each assessment (inclusion visit, 1-month post completion visit and 4-month post completion visit), the 3 sub-dimensions will be analyzed.
The patient must answer the 12 questions with "Never", "Rarely", "Sometimes", "Often" or "Always" (only one answer possible). Each answer is scored from 5 to 1 in this order, except for questions 3, 5 and 7 where the values are reversed. The associated total score varies from 12 to 60. The higher the score, the better the oral quality of life. The score obtained is classified into three categories:
12< <50: poor oral quality of life 51< <56: average oral quality of life 57< <60: good oral quality of life
Measured: 4 months
masticatory muscle activity at the insertion of prostheses in mouth
Measurement of muscle activity = measurements will be made for all muscles at rest with and without prostheses.
Measured: at the insertion of prostheses in mouth
masticatory muscle activity at 4 months of wearing prostheses
Measurement of muscle activity = measurements will be made for all muscles at rest with and without prostheses.
Measured: 4 months
masticatory muscle balance at the insertion of prostheses in mouth
Muscle balance analysis = comparison of right and left muscle activity.
Measured: at the insertion of prostheses in mouth
masticatory muscle balance at 4 months of wearing prostheses
Muscle balance analysis = comparison of right and left muscle activity.
Measured: 4 months
Analysis of the chronology of muscle contraction on the right and left
Analysis of the chronology of muscle contraction on the right and left = muscle contraction symmetry
Measured: 1 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Oct 2021
- Study start25 Feb 2022
- Primary completionFeb 2025 (estimated)
- Study completionAug 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Disorder of Maxillary and Mandibular Dental Arch RelationshipStudies of the same condition, open and under way.
- More trials run by University Hospital, MontpellierThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Montpellier
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Delphine Carayon, MCU-PH, Principal investigator, University Hospital, Montpellier
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05096624
- Sponsor's protocol ID
- RECHMPL20_0407
- Acronym
- DD-TENS
- Status last verified
- Jun 2023
- First submitted
- 15 Oct 2021
- Last updated
- 5 Jul 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Complete Removable Prosthetic Rehabilitations Performed by an Innovative DDTENS Protocol, on the Quality of Masticatory Function and the Management of Completely Edentulous Patients
- ClinicalTrials.gov ID
- NCT05096624
- Acronym / sponsor ID
- DD-TENS / RECHMPL20_0407
- Keywords
- Total bimaxillary edentulous patient, Digital Denture, Neuromuscular occlusion
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- University Hospital, MontpellierUniversity, hospital or other
- Study start
- 25 Feb 2022 (actual)
- Primary completion
- Feb 2025 (estimated)
- Study completion
- Aug 2025 (estimated)
- First posted
- 27 Oct 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Total edentulism is a profound physical, psychic and social handicap, which affects 5 million people in France. The most frequent complaint of edentulous patients rehabilitated by conventional Complete Removable Prostheses (CRP) is the reduction of masticatory efficiency. This alteration has medical repercussions and a negative psychological and social impact.
Our study aims to evaluate the impact of an innovative protocol on the quality of masticatory function, prosthetic treatment and, in fact, on the quality of life of the totally edentulous patient. This protocol combines the Digital Denture system with the transcutaneous electrical neurostimulation system (TENS®), in order to improve the balance of the dento-dental contacts of CRP. This new protocol is called DDTENS.
The first objective of the study is to compare the activity and balance of the masticatory muscles at 1 month (T1) of wearing the prostheses, between an experimental group benefiting from a CRP by the DDTENS protocol and 2 reference groups ( the first benefiting from a CRP by the conventional procedure and the second by the Digital Denture procedure) in bimaxillary total edentulous patients
The secondary objectives are:
- to compare the number of sessions required to obtain a finalized bimaxillary total removable prosthesis between the 3 groups.
- to compare the quality of life of patients with their CRP between the 3 groups, at 1 month and 4 months of wearing the prostheses.
- to compare the activity and balance of the masticatory muscles when the prostheses were put in the mouth (T0) and at 4 months (T4) of wearing the prostheses
The study design is a randomised open-label controlled pilot study with blinded reviewer assessment comparing 3 parallel groups:
- Experimental group: 10 bimaxillary edentulous patients rehabilitated by CRP using the DDTENS protocol.
- Control group 1: 10 edentulous bimaxillary patients rehabilitated by CRP according to the conventional method (gold standard technique).
- Control group 2: 10 edentulous bimaxillary patients rehabilitated by CRP using the Digital Denture procedure.
The expected benefits for patients in the DDTENS experimental group are the optimization of occlusal balance, the optimization of the time of integration of the prosthesis in the mouth, the time saving in the prosthetic treatment of the edentulous patient and the improvement of eating behaviours and quality of life of edentulous patients which would delay the entry of our patients into the sphere of dependence.
These results would allow the validation of a new rehabilitation protocol for the edentulous patient, leading to a modification of clinical practices.
Detailed description
EPIDEMIOLOGY Total edentulism is defined by the total absence of teeth. It can be uni or bimaxillary and represents a profound physical, psychic and social handicap, affecting 5 million people in France. Despite progress in prophylaxis, the number of patients with total edentulism is constantly increasing.
There are several explanations for this phenomenon in France:
- Increase in life expectancy According to INSEE, life expectancy in France will increase from 75.2 years to 89.5 years for men and from 82.7 to 93 years for women between 2000 and 2050.
- Social precarity Social precarity is a societal problem that explains the delay or lack of dental care, leading to a higher rate of total edentulism among the most disadvantaged social class populations. Lifestyle behaviors such as smoking and alcohol consumption worsen this situation.
- Ageing of the population The arrival of the baby boomers in the 60+ age group and the increase in life expectancy explain the inevitable ageing of the population (3). People aged over 60 are expected to represent 1/3 of the population in 2050, whereas in 2005 they represented only 1/5.
This ageing is often associated with an alteration in physical and intellectual faculties. The relative well-being of 60-75 year old is gradually giving way to frailty. The challenge is to care for increasingly elderly edentulous patients. It is therefore essential to develop prosthetic rehabilitation practices to improve patient comfort.
Adopting an adapted treatment by limiting the number of appointments while maintaining an optimal quality of care is one of the objectives of our project.
PROBLEMATIC OF TOTAL EDENTULISM In the totally edentulous patient, certain physiological functions are altered (mastication, swallowing, taste, phonation). The most frequent complaint of edentulous patients rehabilitated by conventional Complete Removable Prosthesis (CRP) is the decrease in masticatory capacity. The masticatory capacity of edentulous patients is equivalent to 1/6 of dentate patients, not to mention the changes in eating behavior with certain foods banned from daily life.
This observation has medical repercussions (nutritional deficiencies, change in eating behavior, risk of misdirection, etc.) and a harmful psychological and social impact.
STATUS OF THE ISSUE Chewing ability can be understood by the shape of the chewing cycle, by bite force or by chewing efficiency. Studies have confirmed that conventional CRP do not restore optimal and efficient masticatory function, due to a lack of precision in the fabrication of the prosthesis and the empirical phase of occlusal balancing. Indeed, the dento-dental contacts, governed by the prosthetic mounting of the teeth, have a major impact on the functioning of the manducatory system.
These functional deficiencies can lead to a loss of physical and psychological autonomy, the gateway to iatrogenic dependence of the elderly in our hospitals.
How to improve masticatory efficiency in the totally edentulous patient? The placement of implants can be an alternative to remedy the problem of CRP retention, but the implant solution is not always feasible.
How to improve masticatory efficiency in the totally edentulous patient without the help of implants? The prosthetic equilibrium of an osteo-muco-portal prosthesis without implants is intimately linked to the tissue equilibrium and the neuro-musculo-articular equilibrium. Conversely, an unstable prosthesis leads to tissue damage and joint disorders.
The stability of the prosthesis is linked to the occlusal balance, the balance of the dento-dental contacts between the two arches. The complexity of the treatment lies in the determination of the inter-arch relationship or maxillo-mandibular relationship (MMR), in the vertical and horizontal directions. Indeed, in the totally edentulous patient, we have no reference points. The only usable determinants are the temporomandibular joints (TMJ).
To date, the conventional therapy or gold standard technique used for the rehabilitation of the totally edentulous patient, consists in recreating a "prosthetic substitution normality" by recording the maxillo-mandibular relationship, by putting the mandible in a reproducible position: the position of centered relation. The definition of the National College of Occlusodontics in 2001 tells us that it corresponds "to the condylar reference situation corresponding to a high, simultaneous condylo-disco-temporal coaptation obtained by non forced control. It is reproducible in a given time and for a given body posture and recordable from a mandibular rotation movement". The problem is that the TMJ is rarely healthy resulting in a more or less empirical and operator-dependent mandibular position. Errors in recording the mandibular position result in a loss of accuracy and an increased number of adjustment sessions.
In 2020, the use of digital tools aims to optimize and improve the recording of useful clinical data, the design and manufacture of a sustainable CRP. At present, no consensus exists but 2 paradigms coexist: the partial use of the digital tool, which punctuates the conventional steps and the use of protocols built entirely around the digital tool. These protocols have emerged secondarily and propose complete systems in 2 or 4 sessions.
Computer Aided Design and Manufacturing (CADCAM) systems applied to the rehabilitation of the totally edentulous patient are called Digital Denture protocols. Although CAD/CAM is a digital tool that has been used for many years in dentistry for the dentate patient, the Digital Denture system is not very widespread at the moment. This system ensures a better adaptation of the complete removable prostheses, thanks to the type of manufacture of the prostheses by machining, and a saving of time during the realization of the prostheses.
All in all, there is still the problem of the precision of the recording of the maxillo-mandibular relationship, which can lead to a number of additional adjustment sessions.
From these clinical findings, the two issues of this project were born:
- How to improve the registration of the maxillomandibular relationship and the accuracy of occlusal balance?
- How to reduce the number of adjustment sessions? Ultimately, the answer to these problems would influence the quality of the masticatory function and consequently the quality of life of the totally edentulous person.
INNOVATION The idea of the DDTENS protocol came from the reflection on the dentate patient with cranio-mandibular dysfunctions. Indeed, a transcutaneous electrical neurostimulation system (TENS®) is used in this clinical case, which allows muscular relaxation and the optimization of dento-dental contacts and thus the rebalancing of bilateral muscular forces.
The innovation consists in setting up an innovative protocol combining 2 existing systems: the Digital Denture system and a neuromuscular and electromyographic approach, via the transcutaneous electrical neurostimulation system (TENS®), in order to improve the registration and balance of dento-dental contacts in CRP.
HYPOTHESIS
- Non-operator depending on the maxillo-mandibular relationship recording with a neuro-musculo-articular reference.
- Reduction in the number of sessions for adjusting the prosthesis.
- Optimization of the prosthetic treatment of edentulous patients.
- Improvement of the occlusal balance and therefore of the quality of the masticatory function of edentulous patients (improvement of mastication, of eating behaviors (impact on nutrition, digestion, etc.), making it possible to delay the entry of our patients into the sphere of dependence.
OBJECTIVES
- Compare, within the framework of a randomized controlled pilot study, the activity and balance of the masticatory muscles at 1 month (T1) of wearing the prostheses, measured by a digital system combining electronic recording of mandibular movements and surface electromyography (K7 Evaluation System®), between an experimental group benefiting from a CRP by the DDTENS protocol and 2 reference groups: the first group benefiting from the performance of a CRP by the conventional procedure and the second by the Digital Denture procedure, in bimaxillary total edentulous patients
- Compare between the 3 groups, the number of sessions necessary to obtain a finalized prosthesis (prostheses are considered finalized when the prostheses worn by the patient are occlusally balanced and do not cause any mucosal injury).
- Compare the quality of life of patients with their PRC (assessment of chewing power, eating behavior, etc.), between the 3 groups, at 1 month and 4 months of wearing the prostheses.
- Compare, between the 3 groups, the activity and balance of the masticatory muscles when the prostheses are put in the mouth (T0) and at 4 months (T4) of wearing the prostheses.
METHODOLOGY The study design is a randomised, open-label, controlled pilot study with blinded reviewer evaluation comparing 3 parallel groups (2 control group and 1 experimental group).
The number of subjects to be included is 30. The randomization will be centralized (Ennov clinical software) and stratified by minimization on sex and age (60-69 and 70-85 years).
The masticatory muscle activity and balance are measured by a digital system combining electronic recording of mandibular movements and surface electromyography system (K7 Evaluation System®)
- Measurement of muscle activity = measurements will be made for all muscles at rest with and without prostheses.
- Muscle balance analysis = comparison of right and left muscle activity.
- Analysis of the chronology of muscle contraction on the right and left = muscle contraction symmetry
The number of sessions required to obtain a finished prosthesis recorded for each patient is listed.
The quality of life of the patients is assessed using a specific oral health measurement questionnaire (GOHAI). The GOHAI includes 12 items with 3 sub-dimensions (functional, psycho-social and pain/discomfort).
For each assessment (inclusion visit, 1-month post completion visit and 4-month post completion visit), the 3 sub-dimensions will be analyzed.
The patient must answer the 12 questions with "Never", "Rarely", "Sometimes", "Often" or "Always" (only one answer possible). Each answer is scored from 5 to 1 in this order, except for questions 3, 5 and 7 where the values are reversed. The associated total score varies from 12 to 60. The higher the score, the better the oral quality of life. The score obtained is classified into three categories:
12< <50: poor oral quality of life 51< <56: average oral quality of life 57< <60: good oral quality of life
ANTICIPATED BENEFITS AND RISKS
The expected benefits for patients in the TENS experimental group are:
- Optimization of maxillomandibular relationship registration
- Optimization of occlusal balance and masticatory functions (dental and muscular)
- Optimization of the integration time of prostheses in the mouth
- Improvement of the eating behaviors and quality of life of edentulous patients
- Time saving in the prosthetic treatment of the edentulous patient
The expected risks are:
- Muscle fatigue during TENS sessions if the application time is longer than 60 minutes.
- Number of adjustment sessions equivalent to the current Digital Denture protocol.
EXPECTED RESULTS AND PERSPECTIVES These results would allow the validation of a new gold standard protocol for the rehabilitation of the edentulous patient, leading to a modification of clinical practices.
Perspectives : This study could serve as the basis for an inter-CHU multicenter study as well as the creation and provision of a database (cohort) for artificial intelligence procedures.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| DD-TENS (Digital Denture-Transcutaneous Electrical Nerve Stimulation) | Experimental | Other: DD-TENS systemPatient with Complete Removable Prostheses according to DD-TENS system |
| Gold standard | Active comparator | Other: Gold StandardPatient with Complete Removable Prostheses according to usual care |
| Digital denture System | Active comparator | Other: Digital Denture systemPatient with Complete Removable Prostheses according to Digital Denture system |
Who may qualify
- Ages
- 60 to 85 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Bimaxillary edentulous patients
- Former bimaxillary CRP wearers (transitional or usage)
- Acceptance of the confiscation of the old prosthesis when the new prosthesis is placed in the mouth and during the 4 months the new prosthesis is worn.
- Signed informed consent
Key exclusion criteria (6 listed)
- Dependent patients (under guardianship or patients in EHPAD)
- Heavy pathologies
- Salivary pathologies (Gougerot-Sjögren syndrome) or asialia related to a medication.
- Patients with a pacemaker
- Skeletal class III with an anteroposterior shift of more than 1 cm
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| DD-TENS systemUse of DD-TENS system | Other | DD-TENS (Digital Denture-Transcutaneous Electrical Nerve Stimulation) |
| Gold StandardGold standard | Other | Gold standard |
| Digital Denture systemUse of Digital Denture system | Other | Digital denture System |
Primary outcome
masticatory muscle activity at 1 month of wearing prostheses
Time frame: 1month
Measurement of muscle activity = measurements will be made for all muscles at rest with and without prostheses.
masticatory muscle balance at 1 month of wearing prostheses
Time frame: 1month
Muscle balance analysis = comparison of right and left muscle activity.
8 secondary outcomes
number of sessions required to obtain a finalized prosthesis
Time frame: 1 month
quality of life of the patients at 1 month of wearing the prosthesis
Time frame: 1 month
quality of life of the patients at 4 months of wearing the prosthesis
Time frame: 4 months
masticatory muscle activity at the insertion of prostheses in mouth
Time frame: at the insertion of prostheses in mouth
masticatory muscle activity at 4 months of wearing prostheses
Time frame: 4 months
masticatory muscle balance at the insertion of prostheses in mouth
Time frame: at the insertion of prostheses in mouth
masticatory muscle balance at 4 months of wearing prostheses
Time frame: 4 months
Analysis of the chronology of muscle contraction on the right and left
Time frame: 1 month
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Jul 2023.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Delphine Carayon, MCU-PH principal investigator
University Hospital, Montpellier
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing DD-TENS system, Gold Standard and Digital Denture system in people with Disorder of Maxillary and Mandibular Dental Arch Relationship, run by University Hospital, Montpellier at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 5 Jul 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Delphine Carayon, MCU-PH (+33467336718, d-carayon@chu-montpellier.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
masticatory muscle activity at 1 month of wearing prostheses (time frame: 1month). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Jul 2023.