Clinical Trials Directory

Trials / Completed

CompletedNCT03552809

Clinical Evaluation of Postoperative Healing After Conventional And Laser Assisted Frenectomy Operations

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Marmara University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The aim of this randomized controlled parallel-designed study was to evaluate clinical healing and patient comfort after conventional and diode laser assisted frenectomy operations in case of high papillary frenulum attachment. Forty-eight patients with high papillary frenulum attachments were included in the study. Patients were randomly divided into three groups; conventional frenectomy operation (Group C), frenectomy operation using diode laser (Group L) and diode laser asissted frenectomy with horizontal incision on the periosteum (Group L+P). Postoperative pain, difficulty in speaking and eating scores were assessed postoperative 3 hours and 1, 7, 14, 21 and 45 days using Visual Analogue Scale (VAS). Evaluation of epithelialization of the wound surface was carried out via hydrogen peroxide to the surface using a dental injector at postoperative 7, 14, 21 and 45 days. Plaque index, gingival index, bleeding on probing and probing depth were assessed at baseline and postoperative 7, 14, 21 and 45 days. All data were compared between groups and within each group.

Conditions

Interventions

TypeNameDescription
DEVICEGigaa Cheese 810 nm Diode LaserDiode Laser assisted frenectomy operation.
PROCEDUREConventional Frenectomy OperationFrenectomy operation performed by surgical blades with suturing.

Timeline

Start date
2016-09-01
Primary completion
2017-10-01
Completion
2017-10-01
First posted
2018-06-12
Last updated
2018-06-12

Source: ClinicalTrials.gov record NCT03552809. Inclusion in this directory is not an endorsement.