Evaluation of the impact of Laser application on postoperative pain and healing of the donor area of Gingival Graft: randomized clinical trial

Not Applicable

• Conditions: Surgery, Oral; G16.762.891

• Registration Number: RBR-8syxj8r
• Lead Sponsor: Faculdade de Odontologia da Universidade Federal de Minas Gerais

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-06-02
• Study Start: 2023-02-06
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Patients over 18 years; periodontal health; to sign of the Declaration of Consent; to present from sites with bleeding to approval of less than 10%.

Exclusion Criteria

Individuals who are diabetic; pregnant and lactating; in need of prophylaxis for bacterial endocarditis; using analgesic or anti-inflammatory medication; smokers.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain, determined through the pain scale (0-10), in the first seven days after surgery. Pain reduction is expected in the test group.

Secondary Outcome Measures

Name	Time	Method
Evaluation of epithelialization - Test with hydrogen peroxide at 4, 7 and 14 days after surgery. Faster epithelialization is expected in the test group.<br><br><br><br>;Bleeding - Clinical evaluation at 1,2,3,4 days after surgery. Decreased bleeding is expected in the test group.;Edema- Clinical evaluation at 1,2,3,4 days after surgery. Decrease in edema is expected in the test group.