FindTrial
Sign In

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

Root coverage of isolated miller class III gingival recessions in the mandible. Randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6r7fh2j
Enrollment
Unknown
Registered
2022-03-15
Start date
2021-11-12
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

periodontics

Interventions

Patients will be randomly allocated and will receive the proposed treatments, 22 patients in the LCT Group (Laterally Closed Tunnel) and 22 in the LPF Group (Laterally Positioned Flap) will be associa
A10.850.710
C07.465.714.258.447

Sponsors

Universidade Federal de Pelotas
Lead Sponsor
Universidade Federal de Pelotas
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.—

Countries

Brazil

Contacts

Public ContactThiago Martins

Universidade Federal de Pelotas

thiagoperio@yahoo.com.br+55(053)32602801

Outcome results

None listed

Source: REBEC (via WHO ICTRP)