Pain Perception and Wound Healing After Laser-assisted Frenectomy in Children

Trakya University

Status: Completed

Conditions: Frenulum; Hypertrophy

Treatments: Device: Laser-assisted frenectomy with 2780 nm Er:Cr;YSGG and 940 nm diode laser

Study type: Interventional

Funder types: Other

Identifiers

NCT04368715

TUTF-BAEK 2019/481

Details and patient eligibility

About

This study is based on the records of the patients treated for labial frenectomy with a dental laser at the Department of Padiatric Dentistry from January 2017 to December 2017. Patients younger than 15 years were included and in total 22 patients who matched the inclusion criteria were investigated in the study. The analyzed data included age, gender, frenelum insertion type, type of dental laser, and postoperative pain perception.

Full description

This study is based on the records of the patients who received laser-assisted frenectomy treatment due to mucogingival problems at pediatric dentistry department during two year period. Twenty-two patients treated with either Er,Cr:YSGG laser 2780 nm or 940 nm diode laser were selected who fulfilled the study's inclusion criteria. The analyzed data included age, gender, frenelum insertion type, type of dental laser, postoperative pain perception and wound healing. Post-operative pain was reported with Wong-Baker Faces Pain Rating Scale after 3 hours 1, 7 and 14 days. Wound surface healing was evaluated through photography. Images were uploaded to the software and the changes in the wound area were measured in square millimeters at the day of frenectomy and on days 1, 7, and 14 postoperatively.

Enrollment: 22 patients

Sex: All

Ages: 8 to 13 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Aged between 8-13
• Patients with high frenulum insertion
• Patients without any systemic condition
• Patients treated with either treated Er:Cr;YSGG or 940 nm diode laser for labial frenectomy
• Patients who were followed up after day 1,7 and 14 for wound healing.
• Patients who were followed up after 3 hours, 1,7,14 days for pain perception

Exclusion criteria

• Patients with systemic condition
• Patients who were not treated with Er:Cr;YSGG or 940 nm diode laser for labial frenectomy
• Patients whose follow up was not properly completed

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

22 participants in 2 patient groups

2780 nm Er:Cr;YSGG laser treated group

Experimental group

Description:

Patients treated with Er:Cr;YSGG laser for labial frenectomy

Treatment:

Device: Laser-assisted frenectomy with 2780 nm Er:Cr;YSGG and 940 nm diode laser

940 nm Diode laser treated group

Experimental group

Description:

Patients treated with 940 nm Diode laser for labial frenectomy

Treatment:

Device: Laser-assisted frenectomy with 2780 nm Er:Cr;YSGG and 940 nm diode laser