Dental Pulp DiseaseRotaPulpNCT04636450
Manual and Rotatory Instrumentation Pulpectomy in Primary Mandibular Molars
A study testing Rotatory technique pulpectomy and Manual pulpectomy in people with Dental Pulp Disease, run by Universidad de Guanajuato at 1 site in Mexico.
Trial summary
In this study, the aim is to compare manual and rotatory pulpectomy techniques on 100 primary mandibular molars on children between the ages of 4 and 8 years. The plan is to conduct a randomized controlled trial with a 1:1 ratio for group allocation at a teaching university pediatric dentistry clinic between January… Read more about this study
- Who is it for?
- Ages 4 to 8 years
- Conditions the study is for
- Dental Pulp Disease
- What is being tested?
- Rotatory technique pulpectomy and Manual pulpectomy
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteMexico
- Study dates
- 8 Dec 2020to 15 Jul 2022
- 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 4 to 8 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Patients between 4 to 8 years old.
- Both genders.
- Patients with an indication for pulpectomy for mandibular molars, based on the of Kuo and colleagues criteria (2006).
- Patients requiring pulpectomy in posterior teeth.
- Adequate dental structure of the crown.
- Patients with a remnant structure of at least two-thirds of the root.
- Patients with a medical file at the Pediatric Dentistry Clinic, Universidad Latinoamericana, Campus Valle.
- Patients with signed informed consent.
Who cannot join
- Patients requiring pulpotomy, extraction, or pulp regeneration therapy.
- Patients who are older than 9 years.
- An unrestorable tooth.
- Internal resorption in the roots visible on radiographs.
- Teeth with mechanical or carious perforations of the floor of the pulp chamber.
- Excessive pathologic root resorption involving more than a third of the root.
Show all 14Show fewer
- Excessive pathologic loss of bone support, with loss of the normal periodontal attachment.
- Presence of a dentigerous or follicular cyst.
- Periapical or interradicular lesion involving the crypt of the developing permanent successor.
- Patients with the diagnosis of molar incisor hypomineralization (MIH).
- Patient's whose legal guardian does not provide their informed consent to participate in this study.
- Uncooperative patients.
- Elimination criteria
- Patients who do not complete the treatment or radiographic follow-up at least at a cut-off point.
Trial locations and contacts
1 site in 1 country.
Mexico1 site, 1 recruiting
- Recruiting
Clínica de Odontopediatría
Mexico City, 03100
Ismael Marin-Merchant, DDS, +5217224201733, i-s-mael3@hotmail.com
Carla F Villasana-Escobedo, DDS, +525573735716, cf.ve_1993@hotmail.com
About this study
Official title: Comparison Between Manual and Rotatory Instrumentation Pulpectomy Treatments in Primary Mandibular Molars
In this study, the aim is to compare manual and rotatory pulpectomy techniques on 100 primary mandibular molars on children between the ages of 4 and 8 years. The plan is to conduct a randomized controlled trial with a 1:1 ratio for group allocation at a teaching university pediatric dentistry clinic between January 2021 and December 2021. Two manual systems, as well as two rotary systems, will be randomly assigned. The adult manual system used will be K-file and the adult rotary system will be K3. The pediatric manual system used in this study will be Kedo-SH, while the pediatric rotary system will be Kedo-S. The observed outcome measures in this study are the following: 1) instrumentation and filling time; 2) filling quality by radiographic evaluation; 3) postoperative pain levels using the visual analog scale at 12 and 24 hours; and 4) frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up.
Read the detailed description
Introduction
Dental caries is a prevalent chronic disease, affecting 60-90% of school-age children in industrialized countries; although in the last four decades the prevalence and severity of caries lesions have decreased, it is still a frequent disease for this age group. The American Dental Association (ADA) classifies dental caries by clinical presentation as initial, moderate, and severe; furthermore, the ADA classifies the disease using the international caries detection and diagnosis system (ICDAS II; International Caries Detection and Assessment System II) and by a radiographic presentation of the proximal faces based on the E0-E2, D1-D3 notation system. Within the non-vital pulp treatments, pulpectomy is indicated in temporary teeth; pulpectomy is a conventional endodontic treatment for teeth with exposed, infected, and/or necrotic tissue to eliminate pulp and periradicular infection.
In a recent systematic review that compared three different strategies for the management of deep caries lesions (i.e. complete caries removal, selective caries removal, and step caries removal), Aïem and colleagues (2020) report an increased restoration failure risk when selective removal is used compared to complete removal of caries. In a study where French dentists were surveyed on the management of deep caries lesions in primary dentition, the majority of respondents mentioned performing deep caries removal in a single step. Endodontic procedures in the pediatric population can assist to keep temporary teeth until exfoliation, which is a key principle of pediatric dentistry. Vital pulp and non-vital pulp treatments are employed in the treatment of severe lesions and deep caries; meanwhile, pulpectomy is a treatment largely used in the primary dentition. In pulp therapy, a pulpotomy is performed by removing the pulp from the chamber, while in a pulpectomy, all the tissue from both the chamber and the root canals is removed.
There are two parameters used to determine root canal treatment success: 1) the morphology and shaping of the canal; and 2) the duct cleanliness or the adequate level of disinfection provided by the type and quantity of intra-canal irrigation (e.g. chlorhexidine, sodium hypochlorite, citric acid, profuse irrigation). A pulpectomy is the technique of choice for primary dentition in deep carious lesions with pulp necrosis since pulpectomy has a higher success rate than pulpotomy. While the time for access to the root canal is less with the use of rotary instrumentation systems compared to a manual technique, manual techniques have the same efficacy as rotary systems in root canal cleaning procedures. Rotary systems have greater clinical success compared to manual techniques, in addition to having advantages in instrumentation time, canal shaping, reduction in working time, better cooperation and less patient fatigue, improvement in the conicity of the root canal, and promoting a higher quality of obturation. In a recent meta-analysis, Manchanda and colleagues (2020) conclude that rotary instrumentation has similar clinical and radiographic success rates to manual techniques in primary dentition; additionally, rotatory techniques show lower levels of postoperative pain and less instrumentation time. In the only study in the Mexican population that compared a rotary system (i.e. K3) against a manual technique (i.e. K-file) it was found that the instrumentation and obturation time was shorter, being a promising technique in children.
Given the limited comparative literature about rotatory techniques used in pulpectomy treatment, it is necessary to conduct clinical trials that compare both manual and rotatory techniques in first dentition treatment. So far, studies have been carried out comparing rotary systems designed for adults in the pediatric population. Recently, interest to validate and implement safe and effective protocols for the management of rotary systems in primary dentition has emerged in pediatric dentistry. Below is a protocol designed to investigate the advantages and disadvantages associated with the use of rotary systems designed for our population of interest.
Study design
Population: patients with pulpectomy indication according to the criteria mentioned by Kuo and colleagues (2006).
Place: Pediatric Dentistry Clinic, Universidad Latinoamericana, Campus Valle.
Time frame: January 2021 - December 2021
Sampling technique: convenience sampling with group randomization.
Study groups: 4 (n= 100 teeth)
- Patients who are treated with a manual pulpectomy and a K-file system.
- Patients who are treated with a manual pulpectomy and a Kedo-SH system.
- Patients who are treated with a rotatory technique pulpectomy and a K3 system.
- Patients who are treated with a rotatory technique pulpectomy and a Kedo-S system.
PICOS framework
P: pediatric population
I: manual system pulpectomy
C: rotary system pulpectomy
O: instrumentation and obturation time, filling quality by radiographic evaluation, postoperative pain levels at 12hr and 24hr, frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up.
S: a randomized controlled trial
Research question
Are there differences between the use of a manual system compared to a rotary system in the pediatric population?
Main objective
Compare the performance between a manual technique and a rotatory technique during biomechanical work.
Particular objectives
- Compare the instrumentation (i.e. during biomechanical work) and filling time between a manual technique and a rotatory technique.
- Compare the filling quality by radiographic evaluation between a manual technique and a rotatory technique at the end of the procedure.
- Compare postoperative pain levels using the visual analog scale at 12 and 24 hours.
- Compare the frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up between the two techniques.
Hypotheses
H1: The rotatory techniques will take less instrumentation and obturation time than the manual techniques.
H1: The quality of the obturation in the rotatory technique will be reported radiographically more frequently as optimal than the manual technique.
H1: The pain levels reported by patients will be lower in the rotatory technique than in the manual technique.
H1: The rotatory technique will have a lower frequency of complications such as fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency at each time point compared to the manual technique.
Statistical analysis
Descriptive statistics will be performed on all variables. Statistical analysis will be performed using SPSS 25 (SPSS Inc., Chicago, IL). All variables will be examined to determine the existence of outliers and whether or not they meet the Gaussian distribution assumption; furthermore, Gaussian distribution will be determined with the Shapiro-Wilk test and by visualizing the data through histograms and Q-Q graphs. The demographic and clinical variables will be summarized in proportions and percentages. Nominal variables will be evaluated with Chi-square tests to assess differences between groups. Categorical variables will be evaluated to determine statistical inferences with the Mann-Whitney test. Continuous variables will be assessed for statistical inferences using t-tests and Levene's test to assess variance equality. Statistical significance will be set at p= 0.05 and a Bonferroni correction will be made for multiple comparisons.
Sample size
The sample size necessary to detect statistically significant differences was calculated by taking the following parameters; α = 0.05 and statistical power of 0.8 (i.e. 1-β). For the calculation of the sample size, the time of instrumentation was used as a measure of clinical outcome. The sample was calculated based on the article by Ochoa-Romero and colleagues (2011) where instrumentation time was used as the primary outcome. The sample calculator used can be found on the website: https://clincalc.com/stats/samplesize.aspx. The calculator designed for two independent groups for continuous variables was selected, using the mean for each group (i.e. group 1: rotatory technique 1.7 minutes ± 0.5; group 2: manual technique 2.5 minutes ± 0.8) taking into account an enrollment 1:1 ratio for this study. The total sample size was 24 teeth (i.e. at least 6 teeth per group to find statistically significant differences in instrumentation time).
- Conditions
- Dental Pulp Disease
- Being tested
- Rotatory technique pulpectomy, Manual pulpectomy
- Keywords
- Pulp therapy, Rotatory system, Primary mandibular molar, Dental pulp cavity
- Medical subject headings
- Dental Pulp Diseases, Dental Caries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Rotatory technique pulpectomyProcedure or surgery
Primary mandibular molars treated with a rotatory technique pulpectomy and a K3 system or a Kedo-S system.
Manual pulpectomyProcedure or surgery
Primary mandibular molars treated with a manual pulpectomy and a K-file system or a Kedo-SH system.
| Study group | Role | What they receive |
|---|---|---|
| Adult manual instrumentation | Active comparator | Primary mandibular molars who are treated with a manual pulpectomy and a K-file system. Receives: Procedure: Manual pulpectomy |
| Pediatric manual instrumentation | Experimental | Primary mandibular molars treated with a manual pulpectomy and a Kedo-SH system. Receives: Procedure: Manual pulpectomy |
| Adult rotatory instrumentation | Active comparator | Primary mandibular molars treated with a rotatory technique pulpectomy and a K3 system. Receives: Procedure: Rotatory technique pulpectomy |
| Pediatric rotatory instrumentation | Experimental | Primary mandibular molars treated with a rotatory technique pulpectomy and a Kedo-S system Receives: Procedure: Rotatory technique pulpectomy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Instrumentation time
The time needed to shape the root canal.
Measured: Minutes; intraoperative time.
Obturation time
Time needed to obturate the root canals.
Measured: Minutes, intraoperative time.
Filling quality
Radiographic evaluation of the root canal filling.
Measured: Immediately after surgical procedure.
Postoperative pain
Pain resulting from the surgical procedure, evaluated with the visual analog pain scale (range, 1 to 10; the higher the score the worst the outcome).
Measured: 12 hours
Postoperative pain
Pain resulting from the surgical procedure, evaluated with the visual analog pain scale (range, 1 to 10; the higher the score the worst the outcome).
Measured: 24 hours
Secondary outcomes (4)
Complications secondary to procedure
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
Measured: 3-months
Complications secondary to procedure
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
Measured: 6-months
Complications secondary to procedure
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
Measured: 9-months
Complications secondary to procedure
Frequency of fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency, among other possible complications
Measured: 12-months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Nov 2020
- Study start8 Dec 2020
- Primary completion15 Dec 2021 (estimated)
- Study completion15 Jul 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (21)Papers the sponsor has linked to this study.
- Other trials for Dental Pulp DiseaseStudies of the same condition, open and under way.
- 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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomized controlled trial
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universidad de Guanajuato
- Sponsor type
- University, hospital or other
- Collaborators
- Universidad Latinoamericana, University Medical Center Groningen
- Responsible party
- Principal investigator, Jaime Daniel Mondragón Uribe, Universidad de Guanajuato
- Investigators
- Benjamín Franco Sánchez, DDS, Principal investigator, Universidad LatinoamericanaMarianela Hernández-Baños, DDS, Principal investigator, Universidad LatinoamericanaJaime D Mondragon, MD, MSc, Principal investigator, University Medical Center Groningen, Universidad de Guanajuato
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04636450
- Sponsor's protocol ID
- ULA-2020-ODP-1
- Acronym
- RotaPulp
- Status last verified
- Dec 2020
- First submitted
- 10 Nov 2020
- Last updated
- 10 Dec 2020
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All anonymized patient data will be made available upon request.
Publications
Aiem E, Joseph C, Garcia A, Smail-Faugeron V, Muller-Bolla M. Caries removal strategies for deep carious lesions in primary teeth: Systematic review. Int J Paediatr Dent. 2020 Jul;30(4):392-404. doi: 10.1111/ipd.12616. Epub 2020 Feb 18.
PubMed 31943437Anusavice KJ. Present and future approaches for the control of caries. J Dent Educ. 2005 May;69(5):538-54.
PubMed 15897335Casas MJ, Kenny DJ, Johnston DH, Judd PL. Long-term outcomes of primary molar ferric sulfate pulpotomy and root canal therapy. Pediatr Dent. 2004 Jan-Feb;26(1):44-8.
PubMed 15080357Crespo S, Cortes O, Garcia C, Perez L. Comparison between rotary and manual instrumentation in primary teeth. J Clin Pediatr Dent. 2008 Summer;32(4):295-8. doi: 10.17796/jcpd.32.4.l57l36355u606576.
PubMed 18767460Frencken JE, Sharma P, Stenhouse L, Green D, Laverty D, Dietrich T. Global epidemiology of dental caries and severe periodontitis - a comprehensive review. J Clin Periodontol. 2017 Mar;44 Suppl 18:S94-S105. doi: 10.1111/jcpe.12677.
PubMed 28266116Fuks AB. Pulp therapy for the primary and young permanent dentitions. Dent Clin North Am. 2000 Jul;44(3):571-96, vii.
PubMed 10925773Fuks, A.B., Guelmann, M., Kupietzky, A. (2012). Current developments in pulp therapy for primary teeth. Endodontic Topics, 23, 50-72. https://doi.org/10.1111/etp.12003
Hecksher F, Vidigal B, Coelho P, Otoni D, Alvarenga C, Nunes E. Endodontic Treatment in Artificial Deciduous Teeth through Manual and Mechanical Instrumentation: A Pilot Study. Int J Clin Pediatr Dent. 2019 Jan-Feb;12(1):15-17. doi: 10.5005/jp-journals-10005-1581.
PubMed 31496565Kaur, R., Singh, R., Sethi, K., Garg, S., Miglani, S. (2014). Review article irrigating solutions in Pediatric Dentistry: literature review and update. J Adv Med Dent Sci, 2, 104- 115.
Kher, M.S., Rao, A. Pulp therapy in primary teeth. Clin Dent Rev 4, 16 (2020). https://doi.org/10.1007/s41894-020-00081-z
Lopes-Fatturi, Aluhê, Souza, Juliana Feltrin de, Menezes, José Vitor Nogara Borges, Fraiz, Fabian Calixto, & Assunção, Luciana Reichert da Silva. (2020). A Survival Analysis of Different Pulp Therapies in Decayed Primary Teeth. Pesquisa Brasileira em Odontopediatria e Clínica Integrada, 20, e4822. Epub April 27, 2020. https://dx.doi.org/10.1590/pboci.2020.038
Manchanda S, Sardana D, Yiu CKY. A systematic review and meta-analysis of randomized clinical trials comparing rotary canal instrumentation techniques with manual instrumentation techniques in primary teeth. Int Endod J. 2020 Mar;53(3):333-353. doi: 10.1111/iej.13233. Epub 2019 Nov 26.
PubMed 31587323Muller-Bolla M, Garcia A, Aiem E, Domejean S. Dentists' decisions for deep carious lesions management in primary teeth. Int J Paediatr Dent. 2020 Sep;30(5):578-586. doi: 10.1111/ipd.12639. Epub 2020 Apr 7.
PubMed 32189409Ochoa-Romero T, Mendez-Gonzalez V, Flores-Reyes H, Pozos-Guillen AJ. Comparison between rotary and manual techniques on duration of instrumentation and obturation times in primary teeth. J Clin Pediatr Dent. 2011 Summer;35(4):359-63. doi: 10.17796/jcpd.35.4.8k013k21t39245n8.
PubMed 22046692Panchal V, Jeevanandan G, Erulappan SM. Comparison between the Effectiveness of Rotary and Manual Instrumentation in Primary Teeth: A Systematic Review. Int J Clin Pediatr Dent. 2019 Jul-Aug;12(4):340-346. doi: 10.5005/jp-journals-10005-1637.
PubMed 31866721
Study at a glance
From the registry record, last updated by the sponsor on 10 Dec 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison Between Manual and Rotatory Instrumentation Pulpectomy Treatments in Primary Mandibular Molars
- ClinicalTrials.gov ID
- NCT04636450
- Acronym / sponsor ID
- RotaPulp / ULA-2020-ODP-1
- Conditions
- Dental Pulp Disease
- Keywords
- Pulp therapy, Rotatory system, Primary mandibular molar, Dental pulp cavity
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Universidad de GuanajuatoUniversity, hospital or other
- Collaborators
- Universidad Latinoamericana, University Medical Center Groningen
- Study start
- 8 Dec 2020 (actual)
- Primary completion
- 15 Dec 2021 (estimated)
- Study completion
- 15 Jul 2022 (estimated)
- First posted
- 19 Nov 2020 (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.
In this study, the aim is to compare manual and rotatory pulpectomy techniques on 100 primary mandibular molars on children between the ages of 4 and 8 years. The plan is to conduct a randomized controlled trial with a 1:1 ratio for group allocation at a teaching university pediatric dentistry clinic between January 2021 and December 2021. Two manual systems, as well as two rotary systems, will be randomly assigned. The adult manual system used will be K-file and the adult rotary system will be K3. The pediatric manual system used in this study will be Kedo-SH, while the pediatric rotary system will be Kedo-S. The observed outcome measures in this study are the following: 1) instrumentation and filling time; 2) filling quality by radiographic evaluation; 3) postoperative pain levels using the visual analog scale at 12 and 24 hours; and 4) frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up.
Detailed description
Introduction
Dental caries is a prevalent chronic disease, affecting 60-90% of school-age children in industrialized countries; although in the last four decades the prevalence and severity of caries lesions have decreased, it is still a frequent disease for this age group. The American Dental Association (ADA) classifies dental caries by clinical presentation as initial, moderate, and severe; furthermore, the ADA classifies the disease using the international caries detection and diagnosis system (ICDAS II; International Caries Detection and Assessment System II) and by a radiographic presentation of the proximal faces based on the E0-E2, D1-D3 notation system. Within the non-vital pulp treatments, pulpectomy is indicated in temporary teeth; pulpectomy is a conventional endodontic treatment for teeth with exposed, infected, and/or necrotic tissue to eliminate pulp and periradicular infection.
In a recent systematic review that compared three different strategies for the management of deep caries lesions (i.e. complete caries removal, selective caries removal, and step caries removal), Aïem and colleagues (2020) report an increased restoration failure risk when selective removal is used compared to complete removal of caries. In a study where French dentists were surveyed on the management of deep caries lesions in primary dentition, the majority of respondents mentioned performing deep caries removal in a single step. Endodontic procedures in the pediatric population can assist to keep temporary teeth until exfoliation, which is a key principle of pediatric dentistry. Vital pulp and non-vital pulp treatments are employed in the treatment of severe lesions and deep caries; meanwhile, pulpectomy is a treatment largely used in the primary dentition. In pulp therapy, a pulpotomy is performed by removing the pulp from the chamber, while in a pulpectomy, all the tissue from both the chamber and the root canals is removed.
There are two parameters used to determine root canal treatment success: 1) the morphology and shaping of the canal; and 2) the duct cleanliness or the adequate level of disinfection provided by the type and quantity of intra-canal irrigation (e.g. chlorhexidine, sodium hypochlorite, citric acid, profuse irrigation). A pulpectomy is the technique of choice for primary dentition in deep carious lesions with pulp necrosis since pulpectomy has a higher success rate than pulpotomy. While the time for access to the root canal is less with the use of rotary instrumentation systems compared to a manual technique, manual techniques have the same efficacy as rotary systems in root canal cleaning procedures. Rotary systems have greater clinical success compared to manual techniques, in addition to having advantages in instrumentation time, canal shaping, reduction in working time, better cooperation and less patient fatigue, improvement in the conicity of the root canal, and promoting a higher quality of obturation. In a recent meta-analysis, Manchanda and colleagues (2020) conclude that rotary instrumentation has similar clinical and radiographic success rates to manual techniques in primary dentition; additionally, rotatory techniques show lower levels of postoperative pain and less instrumentation time. In the only study in the Mexican population that compared a rotary system (i.e. K3) against a manual technique (i.e. K-file) it was found that the instrumentation and obturation time was shorter, being a promising technique in children.
Given the limited comparative literature about rotatory techniques used in pulpectomy treatment, it is necessary to conduct clinical trials that compare both manual and rotatory techniques in first dentition treatment. So far, studies have been carried out comparing rotary systems designed for adults in the pediatric population. Recently, interest to validate and implement safe and effective protocols for the management of rotary systems in primary dentition has emerged in pediatric dentistry. Below is a protocol designed to investigate the advantages and disadvantages associated with the use of rotary systems designed for our population of interest.
Study design
Population: patients with pulpectomy indication according to the criteria mentioned by Kuo and colleagues (2006).
Place: Pediatric Dentistry Clinic, Universidad Latinoamericana, Campus Valle.
Time frame: January 2021 - December 2021
Sampling technique: convenience sampling with group randomization.
Study groups: 4 (n= 100 teeth)
- Patients who are treated with a manual pulpectomy and a K-file system.
- Patients who are treated with a manual pulpectomy and a Kedo-SH system.
- Patients who are treated with a rotatory technique pulpectomy and a K3 system.
- Patients who are treated with a rotatory technique pulpectomy and a Kedo-S system.
PICOS framework
P: pediatric population
I: manual system pulpectomy
C: rotary system pulpectomy
O: instrumentation and obturation time, filling quality by radiographic evaluation, postoperative pain levels at 12hr and 24hr, frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up.
S: a randomized controlled trial
Research question
Are there differences between the use of a manual system compared to a rotary system in the pediatric population?
Main objective
Compare the performance between a manual technique and a rotatory technique during biomechanical work.
Particular objectives
- Compare the instrumentation (i.e. during biomechanical work) and filling time between a manual technique and a rotatory technique.
- Compare the filling quality by radiographic evaluation between a manual technique and a rotatory technique at the end of the procedure.
- Compare postoperative pain levels using the visual analog scale at 12 and 24 hours.
- Compare the frequency of complications (e.g. fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency) after a 3-, 6-, 9-, and 12-month follow-up between the two techniques.
Hypotheses
H1: The rotatory techniques will take less instrumentation and obturation time than the manual techniques.
H1: The quality of the obturation in the rotatory technique will be reported radiographically more frequently as optimal than the manual technique.
H1: The pain levels reported by patients will be lower in the rotatory technique than in the manual technique.
H1: The rotatory technique will have a lower frequency of complications such as fistulas, thinning of the mesiodistal walls, periapical or furcation radiolucency at each time point compared to the manual technique.
Statistical analysis
Descriptive statistics will be performed on all variables. Statistical analysis will be performed using SPSS 25 (SPSS Inc., Chicago, IL). All variables will be examined to determine the existence of outliers and whether or not they meet the Gaussian distribution assumption; furthermore, Gaussian distribution will be determined with the Shapiro-Wilk test and by visualizing the data through histograms and Q-Q graphs. The demographic and clinical variables will be summarized in proportions and percentages. Nominal variables will be evaluated with Chi-square tests to assess differences between groups. Categorical variables will be evaluated to determine statistical inferences with the Mann-Whitney test. Continuous variables will be assessed for statistical inferences using t-tests and Levene's test to assess variance equality. Statistical significance will be set at p= 0.05 and a Bonferroni correction will be made for multiple comparisons.
Sample size
The sample size necessary to detect statistically significant differences was calculated by taking the following parameters; α = 0.05 and statistical power of 0.8 (i.e. 1-β). For the calculation of the sample size, the time of instrumentation was used as a measure of clinical outcome. The sample was calculated based on the article by Ochoa-Romero and colleagues (2011) where instrumentation time was used as the primary outcome. The sample calculator used can be found on the website: https://clincalc.com/stats/samplesize.aspx. The calculator designed for two independent groups for continuous variables was selected, using the mean for each group (i.e. group 1: rotatory technique 1.7 minutes ± 0.5; group 2: manual technique 2.5 minutes ± 0.8) taking into account an enrollment 1:1 ratio for this study. The total sample size was 24 teeth (i.e. at least 6 teeth per group to find statistically significant differences in instrumentation time).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 4
- Model description
- Randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| Adult manual instrumentation | Active comparator | Procedure: Manual pulpectomyPrimary mandibular molars who are treated with a manual pulpectomy and a K-file system. |
| Pediatric manual instrumentation | Experimental | Procedure: Manual pulpectomyPrimary mandibular molars treated with a manual pulpectomy and a Kedo-SH system. |
| Adult rotatory instrumentation | Active comparator | Procedure: Rotatory technique pulpectomyPrimary mandibular molars treated with a rotatory technique pulpectomy and a K3 system. |
| Pediatric rotatory instrumentation | Experimental | Procedure: Rotatory technique pulpectomyPrimary mandibular molars treated with a rotatory technique pulpectomy and a Kedo-S system |
Who may qualify
- Ages
- 4 to 8 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (8 listed)
- Patients between 4 to 8 years old.
- Both genders.
- Patients with an indication for pulpectomy for mandibular molars, based on the of Kuo and colleagues criteria (2006).
- Patients requiring pulpectomy in posterior teeth.
- Adequate dental structure of the crown.
Key exclusion criteria (14 listed)
- Patients requiring pulpotomy, extraction, or pulp regeneration therapy.
- Patients who are older than 9 years.
- An unrestorable tooth.
- Internal resorption in the roots visible on radiographs.
- Teeth with mechanical or carious perforations of the floor of the pulp chamber.
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 |
|---|---|---|
| Rotatory technique pulpectomyPrimary mandibular molars treated with a rotatory technique pulpectomy and a K3 system or a Kedo-S system. | Procedure or surgery | Adult rotatory instrumentation, Pediatric rotatory instrumentation |
| Manual pulpectomyPrimary mandibular molars treated with a manual pulpectomy and a K-file system or a Kedo-SH system. | Procedure or surgery | Adult manual instrumentation, Pediatric manual instrumentation |
Primary outcome
Instrumentation time
Time frame: Minutes; intraoperative time.
The time needed to shape the root canal.
Obturation time
Time frame: Minutes, intraoperative time.
Time needed to obturate the root canals.
Filling quality
Time frame: Immediately after surgical procedure.
Radiographic evaluation of the root canal filling.
Postoperative pain
Time frame: 12 hours
Pain resulting from the surgical procedure, evaluated with the visual analog pain scale (range, 1 to 10; the higher the score the worst the outcome).
Postoperative pain
Time frame: 24 hours
Pain resulting from the surgical procedure, evaluated with the visual analog pain scale (range, 1 to 10; the higher the score the worst the outcome).
4 secondary outcomes
Complications secondary to procedure
Time frame: 3-months
Complications secondary to procedure
Time frame: 6-months
Complications secondary to procedure
Time frame: 9-months
Complications secondary to procedure
Time frame: 12-months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Dec 2020.
- Results publication: PubMed 31943437Aiem E, Joseph C, Garcia A, Smail-Faugeron V, Muller-Bolla M. Caries removal strategies for deep carious lesions in primary teeth: Systematic review. Int J Paediatr Dent. 2020 Jul;30(4):392-404. doi: 10.1111/ipd.12616. Epub 2020 Feb 18.
- Results publication: PubMed 15897335Anusavice KJ. Present and future approaches for the control of caries. J Dent Educ. 2005 May;69(5):538-54.
- Results publication: PubMed 15080357Casas MJ, Kenny DJ, Johnston DH, Judd PL. Long-term outcomes of primary molar ferric sulfate pulpotomy and root canal therapy. Pediatr Dent. 2004 Jan-Feb;26(1):44-8.
- Results publication: PubMed 18767460Crespo S, Cortes O, Garcia C, Perez L. Comparison between rotary and manual instrumentation in primary teeth. J Clin Pediatr Dent. 2008 Summer;32(4):295-8. doi: 10.17796/jcpd.32.4.l57l36355u606576.
- Results publication: PubMed 28266116Frencken JE, Sharma P, Stenhouse L, Green D, Laverty D, Dietrich T. Global epidemiology of dental caries and severe periodontitis - a comprehensive review. J Clin Periodontol. 2017 Mar;44 Suppl 18:S94-S105. doi: 10.1111/jcpe.12677.
- Results publication: PubMed 10925773Fuks AB. Pulp therapy for the primary and young permanent dentitions. Dent Clin North Am. 2000 Jul;44(3):571-96, vii.
- Results publicationFuks, A.B., Guelmann, M., Kupietzky, A. (2012). Current developments in pulp therapy for primary teeth. Endodontic Topics, 23, 50-72. https://doi.org/10.1111/etp.12003
- Results publication: PubMed 31496565Hecksher F, Vidigal B, Coelho P, Otoni D, Alvarenga C, Nunes E. Endodontic Treatment in Artificial Deciduous Teeth through Manual and Mechanical Instrumentation: A Pilot Study. Int J Clin Pediatr Dent. 2019 Jan-Feb;12(1):15-17. doi: 10.5005/jp-journals-10005-1581.
- Results publicationKaur, R., Singh, R., Sethi, K., Garg, S., Miglani, S. (2014). Review article irrigating solutions in Pediatric Dentistry: literature review and update. J Adv Med Dent Sci, 2, 104- 115.
- Results publicationKher, M.S., Rao, A. Pulp therapy in primary teeth. Clin Dent Rev 4, 16 (2020). https://doi.org/10.1007/s41894-020-00081-z
- Results publicationLopes-Fatturi, Aluhê, Souza, Juliana Feltrin de, Menezes, José Vitor Nogara Borges, Fraiz, Fabian Calixto, & Assunção, Luciana Reichert da Silva. (2020). A Survival Analysis of Different Pulp Therapies in Decayed Primary Teeth. Pesquisa Brasileira em Odontopediatria e Clínica Integrada, 20, e4822. Epub April 27, 2020. https://dx.doi.org/10.1590/pboci.2020.038
- Results publication: PubMed 31587323Manchanda S, Sardana D, Yiu CKY. A systematic review and meta-analysis of randomized clinical trials comparing rotary canal instrumentation techniques with manual instrumentation techniques in primary teeth. Int Endod J. 2020 Mar;53(3):333-353. doi: 10.1111/iej.13233. Epub 2019 Nov 26.
- Individual participant dataSharing planned: Yes. All anonymized patient data will be made available upon request.
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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.
Benjamín Franco Sánchez, DDS principal investigator
Universidad Latinoamericana
Marianela Hernández-Baños, DDS principal investigator
Universidad Latinoamericana
Jaime D Mondragon, MD, MSc principal investigator
University Medical Center Groningen, Universidad de Guanajuato
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Rotatory technique pulpectomy and Manual pulpectomy in people with Dental Pulp Disease, run by Universidad de Guanajuato at 1 site in Mexico.
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 8 inclusion and 14 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 10 Dec 2020. 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 Mexico. 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 Marianela Hernández-Baños, DDS (+525545600120, neladentist@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Instrumentation time (time frame: Minutes; intraoperative time.). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04636450, which also lists 21 linked publications.
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 10 Dec 2020.