Root coverage of isolated gingival recessions with loss of interproximal tissues in the mandible

Not Applicable

Recruiting

• Conditions: periodontics; surgical flaps; C07.465.714.258.447; F02.463.785.477

• Registration Number: RBR-6r7fh2j
• Lead Sponsor: niversidade Federal de Pelotas

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-03-15
• Last Update Posted: 29 May 2023
• Study Completion: 2024-11-12

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Age over 18 years old;
No contraindications for performing surgical procedures, including the need for antibiotic therapy prior to dental procedures;
Have not performed previous surgeries in the involved sites;
Patients with good oral hygiene (IPV and ISG < 20%);
Patients with isolated Miller Class III GR in the mandible, located in the incisors, canines or premolars;
Well identifiable presence of the cementoenamel junction (CEJ).

Exclusion Criteria

Systemically compromised patients;
Pregnant or lactating women;
Teeth with presence of abrasion, decay, crowns or restorations involving the root;
Molars with Miller's Class III GR;
Teeth with Miller Class III GR without the well-identified presence of JCE.
Patients who are smokers or ex-smokers who have stopped smoking for less than a year.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
All examinations will be repeated by the same trained examiner who is blinded to the type of treatment applied after 10 days, 1, 3 and 6 months. The primary outcome will be the percentage of complete root coverage.

Secondary Outcome Measures

Name	Time	Method
All examinations will be repeated by the same trained examiner who is blinded to the type of treatment applied after 10 days, 1, 3 and 6 months. The secundary outcomes will be the percentage of root coverage, clinical attachment level gain, probing depth and keratinized tissue gain in the region and oral health-related quality of life (QVRSB). In addition, 3, 7 and 10 days after the procedures are carried out, the patients' postoperative pain will be measured.