Recession, Gingival Clinical Trial
Official title:
Clinical Evaluation of Laterally Closed Tunnel Technique Versus Coronally Advanced Flap Combined With Connective Tissue Graft for the Treatment of Isolated RT2 Gingival Recession: A Randomized Controlled Clinical Trial
NCT number | NCT05823415 |
Other study ID # | 1241953 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | April 2023 |
Est. completion date | March 2024 |
Verified date | April 2023 |
Source | British University In Egypt |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this study is to evaluate reduction of recession depth using lateral closed tunnel technique versus CAF technique using connective tissue graft in single RT2 gingival recession cases.
Status | Not yet recruiting |
Enrollment | 22 |
Est. completion date | March 2024 |
Est. primary completion date | March 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - Single RT2 buccal gingival recession = 2 mm in the esthetic zone (Gingival recession associated with loss of inter-proximal attachment. The amount of interproximal attachment loss (measured from the interproximal CEJ to the depth of the interproximal pocket) was less than or equal to the buccal attachment loss (measured from the buccal CEJ to the depth of the buccal pocket) - Patients with good oral hygiene - Medically free patients - No signs of active periodontal disease (with no site showing probing depth > 4 mm and full-mouth bleeding score (FMBS) 20% (measured at four sites per tooth). - Palate with sufficient thickness to accommodate soft tissue defect. Exclusion Criteria: - Smokers - Pregnancy - Severe gag reflex - Non-carious cervical lesion - History of mucogingival or periodontal surgery at the experimental site - History of medication that can affect periodontal healing |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
British University In Egypt |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction in recession depth | 6 Months | ||
Secondary | Post-operative pain assessed by VAS Scale | Pain score reported by the patient directly through Visual Analogue Scale score (between 0 and 10, 0: no pain, 1: minimal pain 5: moderate pain, 10: severe pain) | 2 week | |
Secondary | Probing Depth | 6 months | ||
Secondary | Clinical Attachment Level | will be measured by a periodontal probe | 6 months | |
Secondary | Width of Keratinized Tissue | 6 months | ||
Secondary | Gingival Thickness | 6 months | ||
Secondary | Percentage of complete root coverage by williams periodontal probe | Preoperative vertical recession - Postoperative vertical recession/preoperative vertical recession) x 100 | 6 months |
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