- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03716752
Modified Connective Tissue Graft Wall With Wing Technique for Posterior Teeth
October 24, 2018 updated by: nermin mohammed ahmed yussif, Cairo University
Modified Connective Tissue Graft Wall With Wing Technique for Posterior Teeth in Treating One Wall Vertical Bone Defects With Class III Gingival Recession: A 12 Months Follow up
The investigators reported here the application of usage modified connective tissue graft wall technique for posterior teeth.
The treatment outcomes suggested the efficacy of the used technique in treating recession defects accompanied by infrabony defects in molars.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Gingival recession is defined as the apical migration of the gingival margin leaving the root surface denuded.
Treatment of Class III and IV defects and achievement good of results seems to be quite difficult due to the advanced loss of the soft and hard tissues supporting the affected teeth.
Furthermore, partial to total loss of the interproximal papilla is one of the main challenges that contribute for achieving higher levels of esthetics especially in anterior zone.
In such a case, conventional techniques of root coverage results usually in poor prognosis.
Study Type
Interventional
Enrollment (Actual)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Giza, Egypt
- Octobar University of Modern Sciences and Arts
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- recession defects in posterior teeth
- vertical infrabony defects in relation to the same recession defect
Exclusion Criteria:
- smokers
- suystemic diseases
- pregnency and lactating mothers
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: bone graft and collagen barrier
peridoontal regeneration using bone graft and collagen barrier as treatment of vertical bony defects with recession defect
|
the usage of bone graft and collagen barrier to treat recession defects accompanied vertical bony defcets in posterior teeth
Other Names:
|
|
Experimental: Modified connective tissue graft wall with wing technique
peridoontal regeneration using bone graft and modified connective tissue graft wall with wing as treatment of vertical bony defects with recession defect
|
the usage of bone graft and collagen barrier to treat recession defects accompanied vertical bony defcets in posterior teeth
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
recession defect dimensions
Time Frame: 12 months
|
measurment of recession defect depth and width
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2016
Primary Completion (Actual)
April 1, 2018
Study Completion (Actual)
June 1, 2018
Study Registration Dates
First Submitted
October 13, 2018
First Submitted That Met QC Criteria
October 22, 2018
First Posted (Actual)
October 23, 2018
Study Record Updates
Last Update Posted (Actual)
October 25, 2018
Last Update Submitted That Met QC Criteria
October 24, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1235
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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