Edentulous JawNCT06127017
Comparing Marginal Bone Loss for Immediately Loaded Implants in Maxillary Full Arch Interim Prosthesis Using Welded Titanium Bar Versus Polyetheretherketone Bar
A study testing splinting dental implants with titanium bar and splinting dental implants with PEEK bar in people with Edentulous Jaw, run by Ain Shams University.
Trial summary
Fourteen completely edentulous patients will be randomly allocated into two parallel arm groups. For both groups virtual implant planning will be done and surgical guide will be planned and printed. An immediate interim full arch PMMA prosthesis will be virtually designed and printed for both groups. Read more about this study
- Who is it for?
- Ages 40 to 70 yearsHealthy volunteers can take part
- Conditions the study is for
- Edentulous Jaw
- What is being tested?
- splinting dental implants with titanium bar and splinting dental implants with PEEK bar
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 14 participants
- Where
- No sites listed yet
- Study dates
- 1 Dec 2023to 1 Aug 2024
- 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 40 to 70 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- .medically free. .class I maxillomandibular relation. .normal salivary flow.
- residual ridge has adequate mucosa
- covered with firm healthy mucosa.
Who cannot join
- . poor oral hygiene. .uncooperative patients. .patients with abnormal oral habits.
Trial locations and contacts
No sites are listed yet.
About this study
Fourteen completely edentulous patients will be randomly allocated into two parallel arm groups. For both groups virtual implant planning will be done and surgical guide will be planned and printed. An immediate interim full arch PMMA prosthesis will be virtually designed and printed for both groups. For the Intraoral welding group, seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by intraoral welded bar. While for PEEK group in which seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by PEEK bar. Marginal bone loss will be clinically evaluated at four, six months follow up period using CBCT.
Read the detailed description
Study settings The study will be conducted in Oral \& Maxillofacial Prosthodontics Department, Faculty of Dentistry, Ain Shams University. Sample size calculation Fourteen patients will be selected to share in this study from the outpatient clinic of Prosthodontics Department, Faculty of Dentistry, Ain-Shams University. G power program (3. 1) was used for calculations of sample size. Statistical calculator was based on 95% confidence interval and power of the study 80% with α error 5%.
Based on a previous study (Degidi, Marco, Diego Nardi, and Adriano Piattelli. "Prospective study with a 2-year follow-up on immediate implant loading in the edentulous mandible with a definitive restoration using intra-oral welding), which showed that the mean of marginal bone growth was 0.21 in one group compared to the second group. Using un paired t test the results were found to be significant. So, it was relied upon in this study. Based on this assumption, sample size was calculated according to these values producing a minimal sample size of fourteen patients being enough to find such a difference. Study procedures
- Randomization and allocation concealment techniques Computer-generated random numbers will be used for simple randomization of the subjects. Therefore, the participants will be randomly allocated into two groups: intraoral welding group and PEEK group. The allocation ration will be set 1:1. Allocation concealment will be done using opaque sealed envelopes.
- Details of intervention:
Ethical approval will be granted by the Research Ethical Committee, Faculty of Dentistry, Ain Shams University (FDASUREC). All patients will be informed in details about the nature of investigation and the aim of the study. Patient's data will be kept safe and confidential to protect the security and privacy of the patient information. All participants will be given notice about their privacy and their rights. 1-Patient Grouping: Fourteen patients will be enrolled in this study and randomly divided into two groups as follow Group Ⅰ: seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by intraoral welded bar. Group Ⅱ: seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by PEEK bar
2-Patient selection: The inclusion criteria will be systemically free completely edentulous patient ranged from 45 y to 69 years old with Class I maxillary-mandibular relationship, Normal salivary flow with normal viscosity. Residual maxillary ridge has adequate bone and covered by firm healthy mucosa. The excluded patients will include patients with major systemic diseases that may affect osseointegration as uncontrolled diabetes or under bisphosphonate treatment, Patients with poor oral hygiene. Patients with abnormal oral habits as (bruxism, clenching, tongue thrusting).Potentially uncooperative patients who are not willing to go through the proposed interventions. 3-Clinical steps:
- pre-surgical procedures: i. Patients' history: Medical history: Patients will be asked about their medical and dental history through a direct interview and a detailed questionnaire sheet. Dental history: Patients will be asked about the cause, the date of teeth extraction and if there is any previous experience with any prosthetic appliance, any problems with TMJ will also be recorded. ii. Patients' examination:
Extra oral examination:
Extraoral examination will be performed for the detection of any abnormal facial anomalies, skin inflammation or lesions, any abnormalities in the TMJ as joint clicking, limitation in mouth opening or pain, and checking the maxillo-mandibular relationship Intra-oral examination: Visual and digital examination will be performed following routine procedures to examine denture bearing mucosa, border tissues, abnormal soft tissue, tongue, frenula, muscle tone, saliva, tori, sharp bony spicules, remaining teeth, arch relationship, ridge form, inter-ridge space and undercuts..
Radiographic evaluation:
(CBCT) radiograph will be done to evaluate the degree of bone resorption, quality and quantity of bone, to detect if there are remaining roots and any pathological lesions
Prosthetic procedures:
Properly constructed conventional single upper denture will be made for all patients. The Conventional denture will be duplicated with radiopaque markers and CBCT will be used to determine the exact positions of the implants. Virtual implant planning will be done using the BlueSky Bio 4 software. A surgical guide will be planned and then the 3D virtual guide will be exported as STL file to the 3D printing machine. An immediate interim full arch PMMA prosthesis will be virtually designed and printed for both groups. For the second group a PEEK bar will be virtually designed and printed. b. Surgical procedure: Surgery will be done under local anesthesia. The surgical guide will be fixed in place. Six implants will be placed according to the planned cone beam CT using surgical guide to accurately place the implants. Implants will be distributed following the Misch protocol; two implants in the first molar position, two implants in the canines position and two implants in the first centrals position. Serial osteotomies will be performed using sharp drills under copious irrigation to decrease heat generation until the planned depth and width will be reached.
The implant will be inserted through the osteotomy manually then continued using a ratchet with 35 Ncm torque Multiunit abutments will be screwed to the implants according to the Virtual implant planning. Titanium cylinders will be connected to the multiunit abutments.
Adjustment of the interim prosthesis and immediate loading:
All the pick-up procedures will be done in the same session of implant installation for both groups.
- For the intraoral welding group: A titanium bar will be welded to titanium cylinders using an intraoral welding unit. Then, pick up will be done for the printed interim PMMA prosthesis to the titanium bar.
- For the PEEK group:
The virtually designed and printed PEEK bar will be cemented to the titanium cylinders using flowable composite then, pick up will be done for the printed interim PMMA prosthesis to the printed PEEK bar. 4-Method of evaluation: Implant marginal bone loss (MBL) will be the difference in marginal bone level from the functional loading time with the interim prosthesis (T0) to the end of the follow-up (T1after four months, T2 after six months) .Marginal bone level around the implant will be measured from the CBCT scans made at T0, T1, T2. Vertical buccal or lingual bone heights (VBBH or VLBH) and horizontal buccal or lingual bone thicknesses (HBBT or HLBT) at the implant platform will be measured at themidsagittal cut of each implant perpendicular to the dental arch on the CBCT scan.
The distance from the implant platform (the horizontal interface between the abutment and the implant) to the most coronal point of bone-to-implant contact will be taken as the vertical bone height. Measurements will be calibrated by using the actual known length of the implant. Similarly, the vertical mesial or distal bone height (VMBH or VDBH) at the implant platform will be measured at the midsagittal cut of each implant parallel to the dental arch on the CBCT scan
- Conditions
- Edentulous Jaw
- Being tested
- splinting dental implants with titanium bar, splinting dental implants with PEEK bar
- Keywords
- immediate loading, interim prosthesis, intra oral welding
- Medical subject headings
- Jaw, Edentulous
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
splinting dental implants with titanium barProcedure or surgery
splinting of dental implants will be done in the placebo comparator group by welding a titanium bar intraorally to the temporary sleeves attached to the implants.
splinting dental implants with PEEK barProcedure or surgery
in the active comparator group ,the PEEK bar will be attached to the temporary sleeves using flowable composite resin material.
| Study group | Role | What they receive |
|---|---|---|
| Titanium bar | Placebo comparator | 6 implants in each participant will be immediately loaded and splinted with intraorally welded titanium bar. Receives: Procedure: splinting dental implants with titanium bar |
| PEEK bar | Active comparator | 6 implants in each participant will be immediately loaded and splinted with PEEK bar. Receives: Procedure: splinting dental implants with PEEK bar |
What is being measured
The primary outcome is the main question the study is designed to answer.
marginal bone loss measurement
marginal bone loss will be measured using cone beam computed tomography at the buccal, palatal, mesial and distal aspect of the implant and an average value will be calculated for each implant.
Measured: total frame of 6 months with the following frequencies :at base line, after 4 months and after 6 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Nov 2023
- Study start1 Dec 2023 (estimated)
- Primary completion1 Aug 2024 (estimated)
- Study completion1 Aug 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Edentulous JawStudies 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
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 14 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ain Shams University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, soha saeid mohammed, Ain Shams University
- Investigators
- soha s elsaeid, Principal investigator, Assistant lecturer ,Faculty of Dentistry, Ain Shams university
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06127017
- Sponsor's protocol ID
- 1226
- Status last verified
- Nov 2023
- First submitted
- 7 Nov 2023
- Last updated
- 24 Nov 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparing Marginal Bone Loss for Immediately Loaded Implants in Maxillary Full Arch Interim Prosthesis Using Welded Titanium Bar Versus Polyetheretherketone Bar
- ClinicalTrials.gov ID
- NCT06127017
- Acronym / sponsor ID
- 1226
- Conditions
- Edentulous Jaw
- Keywords
- immediate loading, interim prosthesis, intra oral welding
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 14 participants (estimated)
- Lead sponsor
- Ain Shams UniversityUniversity, hospital or other
- Study start
- 1 Dec 2023 (estimated)
- Primary completion
- 1 Aug 2024 (estimated)
- Study completion
- 1 Aug 2024 (estimated)
- First posted
- 13 Nov 2023 (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.
Fourteen completely edentulous patients will be randomly allocated into two parallel arm groups. For both groups virtual implant planning will be done and surgical guide will be planned and printed. An immediate interim full arch PMMA prosthesis will be virtually designed and printed for both groups. For the Intraoral welding group, seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by intraoral welded bar. While for PEEK group in which seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by PEEK bar. Marginal bone loss will be clinically evaluated at four, six months follow up period using CBCT.
Detailed description
Study settings The study will be conducted in Oral \& Maxillofacial Prosthodontics Department, Faculty of Dentistry, Ain Shams University. Sample size calculation Fourteen patients will be selected to share in this study from the outpatient clinic of Prosthodontics Department, Faculty of Dentistry, Ain-Shams University. G power program (3. 1) was used for calculations of sample size. Statistical calculator was based on 95% confidence interval and power of the study 80% with α error 5%.
Based on a previous study (Degidi, Marco, Diego Nardi, and Adriano Piattelli. "Prospective study with a 2-year follow-up on immediate implant loading in the edentulous mandible with a definitive restoration using intra-oral welding), which showed that the mean of marginal bone growth was 0.21 in one group compared to the second group. Using un paired t test the results were found to be significant. So, it was relied upon in this study. Based on this assumption, sample size was calculated according to these values producing a minimal sample size of fourteen patients being enough to find such a difference. Study procedures
- Randomization and allocation concealment techniques Computer-generated random numbers will be used for simple randomization of the subjects. Therefore, the participants will be randomly allocated into two groups: intraoral welding group and PEEK group. The allocation ration will be set 1:1. Allocation concealment will be done using opaque sealed envelopes.
- Details of intervention:
Ethical approval will be granted by the Research Ethical Committee, Faculty of Dentistry, Ain Shams University (FDASUREC). All patients will be informed in details about the nature of investigation and the aim of the study. Patient's data will be kept safe and confidential to protect the security and privacy of the patient information. All participants will be given notice about their privacy and their rights. 1-Patient Grouping: Fourteen patients will be enrolled in this study and randomly divided into two groups as follow Group Ⅰ: seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by intraoral welded bar. Group Ⅱ: seven patients will receive immediately loaded interim fixed full arch prosthesis splinted by PEEK bar
2-Patient selection: The inclusion criteria will be systemically free completely edentulous patient ranged from 45 y to 69 years old with Class I maxillary-mandibular relationship, Normal salivary flow with normal viscosity. Residual maxillary ridge has adequate bone and covered by firm healthy mucosa. The excluded patients will include patients with major systemic diseases that may affect osseointegration as uncontrolled diabetes or under bisphosphonate treatment, Patients with poor oral hygiene. Patients with abnormal oral habits as (bruxism, clenching, tongue thrusting).Potentially uncooperative patients who are not willing to go through the proposed interventions. 3-Clinical steps:
- pre-surgical procedures: i. Patients' history: Medical history: Patients will be asked about their medical and dental history through a direct interview and a detailed questionnaire sheet. Dental history: Patients will be asked about the cause, the date of teeth extraction and if there is any previous experience with any prosthetic appliance, any problems with TMJ will also be recorded. ii. Patients' examination:
Extra oral examination:
Extraoral examination will be performed for the detection of any abnormal facial anomalies, skin inflammation or lesions, any abnormalities in the TMJ as joint clicking, limitation in mouth opening or pain, and checking the maxillo-mandibular relationship Intra-oral examination: Visual and digital examination will be performed following routine procedures to examine denture bearing mucosa, border tissues, abnormal soft tissue, tongue, frenula, muscle tone, saliva, tori, sharp bony spicules, remaining teeth, arch relationship, ridge form, inter-ridge space and undercuts..
Radiographic evaluation:
(CBCT) radiograph will be done to evaluate the degree of bone resorption, quality and quantity of bone, to detect if there are remaining roots and any pathological lesions
Prosthetic procedures:
Properly constructed conventional single upper denture will be made for all patients. The Conventional denture will be duplicated with radiopaque markers and CBCT will be used to determine the exact positions of the implants. Virtual implant planning will be done using the BlueSky Bio 4 software. A surgical guide will be planned and then the 3D virtual guide will be exported as STL file to the 3D printing machine. An immediate interim full arch PMMA prosthesis will be virtually designed and printed for both groups. For the second group a PEEK bar will be virtually designed and printed. b. Surgical procedure: Surgery will be done under local anesthesia. The surgical guide will be fixed in place. Six implants will be placed according to the planned cone beam CT using surgical guide to accurately place the implants. Implants will be distributed following the Misch protocol; two implants in the first molar position, two implants in the canines position and two implants in the first centrals position. Serial osteotomies will be performed using sharp drills under copious irrigation to decrease heat generation until the planned depth and width will be reached.
The implant will be inserted through the osteotomy manually then continued using a ratchet with 35 Ncm torque Multiunit abutments will be screwed to the implants according to the Virtual implant planning. Titanium cylinders will be connected to the multiunit abutments.
Adjustment of the interim prosthesis and immediate loading:
All the pick-up procedures will be done in the same session of implant installation for both groups.
- For the intraoral welding group: A titanium bar will be welded to titanium cylinders using an intraoral welding unit. Then, pick up will be done for the printed interim PMMA prosthesis to the titanium bar.
- For the PEEK group:
The virtually designed and printed PEEK bar will be cemented to the titanium cylinders using flowable composite then, pick up will be done for the printed interim PMMA prosthesis to the printed PEEK bar. 4-Method of evaluation: Implant marginal bone loss (MBL) will be the difference in marginal bone level from the functional loading time with the interim prosthesis (T0) to the end of the follow-up (T1after four months, T2 after six months) .Marginal bone level around the implant will be measured from the CBCT scans made at T0, T1, T2. Vertical buccal or lingual bone heights (VBBH or VLBH) and horizontal buccal or lingual bone thicknesses (HBBT or HLBT) at the implant platform will be measured at themidsagittal cut of each implant perpendicular to the dental arch on the CBCT scan.
The distance from the implant platform (the horizontal interface between the abutment and the implant) to the most coronal point of bone-to-implant contact will be taken as the vertical bone height. Measurements will be calibrated by using the actual known length of the implant. Similarly, the vertical mesial or distal bone height (VMBH or VDBH) at the implant platform will be measured at the midsagittal cut of each implant parallel to the dental arch on the CBCT scan
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Titanium bar | Placebo comparator | Procedure: splinting dental implants with titanium bar6 implants in each participant will be immediately loaded and splinted with intraorally welded titanium bar. |
| PEEK bar | Active comparator | Procedure: splinting dental implants with PEEK bar6 implants in each participant will be immediately loaded and splinted with PEEK bar. |
Who may qualify
- Ages
- 40 to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- .medically free. .class I maxillomandibular relation. .normal salivary flow.
- residual ridge has adequate mucosa
- covered with firm healthy mucosa.
Key exclusion criteria (1 listed)
- . poor oral hygiene. .uncooperative patients. .patients with abnormal oral habits.
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 |
|---|---|---|
| splinting dental implants with titanium barsplinting of dental implants will be done in the placebo comparator group by welding a titanium bar intraorally to the temporary sleeves attached to the implants. | Procedure or surgery | Titanium bar |
| splinting dental implants with PEEK barin the active comparator group ,the PEEK bar will be attached to the temporary sleeves using flowable composite resin material. | Procedure or surgery | PEEK bar |
Primary outcome
marginal bone loss measurement
Time frame: total frame of 6 months with the following frequencies :at base line, after 4 months and after 6 months.
marginal bone loss will be measured using cone beam computed tomography at the buccal, palatal, mesial and distal aspect of the implant and an average value will be calculated for each implant.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Nov 2023.
- Individual participant dataSharing planned: No
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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.
soha s elsaeid principal investigator
Assistant lecturer ,Faculty of Dentistry, Ain Shams university
Questions about this trial
What is this clinical trial studying?
A study testing splinting dental implants with titanium bar and splinting dental implants with PEEK bar in people with Edentulous Jaw, run by Ain Shams University.
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 3 inclusion and 1 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 24 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. 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 soha s elsaeid (01066747918 ext. 002, sohasaeid@dent.asu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
marginal bone loss measurement (time frame: total frame of 6 months with the following frequencies :at base line, after 4 months and after 6 months.). 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 24 Nov 2023.