Comparing diode laser and scalpel techniques for frenectomy
Evaluation of Patients' Perceptions and Soft Tissue Changes After Conventional and Diode Laser Frenectomy
This study is testing whether using a diode laser or a scalpel for frenectomy helps adults with high frenum attachment feel less pain and heal better after the procedure.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 43 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | All |
| Sponsor | Necmettin Erbakan University Academic / other |
| Locations | 1 site (Konya) |
| Trial ID | NCT06548516 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of diode laser treatment versus conventional scalpel techniques for frenectomy in adults with high frenum attachment. It will assess post-operative pain levels and periodontal healing outcomes in participants aged 18-45 who are systemically healthy and non-smokers. A total of 43 participants will be randomly assigned to either the diode laser group or the scalpel group, with their pain and healing monitored at baseline, 6 weeks, and 6 months post-operation. The study will utilize a single-blind design to ensure unbiased results.
Who should consider this trial
Good fit: Ideal candidates are systemically healthy, non-smoking adults aged 18-45 with aberrant papillary frenum attachment.
Not a fit: Patients with systemic diseases affecting wound healing, smokers, or those on certain medications may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved post-operative outcomes and reduced pain for patients undergoing frenectomy.
How similar studies have performed: Previous studies have shown promising results with laser techniques in dental procedures, suggesting potential benefits, though this specific comparison is less commonly tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Systemically healthy * Nonsmoker * No periodontal treatment received in the last 3 months * Having at least 20 teeth * Presence of at least central incisors, lateral incisors, and canines in the maxilla * Not pregnant or breastfeeding * No psychiatric, mental, or physical impairments * Diagnosed with gingival health based on the "World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions * Consent to participate in the study. Exclusion Criteria: * Any systemic disease that could interfere with the wound healing process (e.g., diabetes mellitus and HIV infection) * Smoking * Use of antibiotics, anti-inflammatory drugs, or any other medication in the last 6 months that could affect the study's outcome * Any hypersensitivity reactions to paracetamol * Any physical limitations or restrictions that could impede normal oral hygiene procedures.
Where this trial is running
Konya
- Necmettin Erbakan University, dentistry Faculty — Konya, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: zeynep taştan eroğlu — Necmettin Erbakan University
- Study coordinator: zeynep taştan eroğlu
- Email: dt.zeyneptastan@gmail.com
- Phone: 00905065857095
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.