Intraoral scans to determine volume change and coverage rate after coverage of singular gingival recessions using free connective tissue graft: a pilot study.
- Conditions
- K05.2K05.3Acute periodontitisChronic periodontitis
- Registration Number
- DRKS00028586
- Lead Sponsor
- Klinik für Zahnerhaltungskunde und Parodontologie, Universitätsklinikum Freiburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 5
Inclusion Criteria
Patients will be operated independently of the study as part of the surgical course of the master's program in periodontology and implant therapy at the University of Freiburg. / The minimum age of patients is 18 years. / Patients must be non-smokers or former smokers. / Informed consent must be obtained. / Patients must have at least one Cairo class RT 1 gingival recession for which treatment by envelope technique is indicated (e.g. due to severe dentin hypersensitivity) / Patients must be instructed in individual oral hygiene and have good oral hygiene (PI = 1 [Silness & Löe 1964]).
Exclusion Criteria
Contraindication to performing an intraoral scan (e.g. epilepsy)
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean and complete root coverage in %.
- Secondary Outcome Measures
Name Time Method -Ratio of the size of the removed connective tissue graft and the recession depth to the postoperative coverage rate in % after 6 and 12 months.<br><br>-Volume increase of the tissue in mm3 in the recession region after 6 and 12 months