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Comparison between Conventional and Paralleling frenectomy techniques

Phase 4
Not yet recruiting
Conditions
Other specified disorders of gingiva and edentulous alveolar ridge,
Registration Number
CTRI/2023/05/052185
Lead Sponsor
maharshtra institute of dental sciences
Brief Summary

The study will be conducted in a clinical settings of department of periodontics on patients diagnosed with papillary type of frenal attachment. It is a randomized clinical trial with parallel arm in which participants will be allocated into two groups i.e. Group I - Frenectomy with Conventional technique, Group II - Frenectomy with Paralleling technique. Patients fulfilling the inclusion criteria and signing the informed consent will be included. Treatment outcomes will be evaluated in terms of clinical parameters at 1 and 3 months post surgery.

Clinical parameters - Evaluation of frenum position, early wound healing score, Pain experienced, Oral hygiene status

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Inclusion criteria: 1.
  • Both male and female with ages ranging from 18-50 years.
  • Systemically healthy subjects 3.
  • Periodontally healthy, Stage I periodontitis patients (periodontal pocket < 4 mm in relation to maxillary anterior teeth) 4.
  • Subjects with no bleeding disorders or allergy to any drugs 5.
  • Papillary type of frenal attachment (according to Placek Mirko classification of frenum).
Exclusion Criteria
  • Exclusion criteria : 1.
  • History of antibiotics, anti-inflammatory or any other drugs that alter wound healing in the last one month.
  • History of any periodontal surgical procedure in the last six months in the concerned area.
  • Pregnant women, lactating females and women taking oral contraceptive pills.
  • Subjects who are smokers and consume tobacco in any form 5.
  • Medically compromised patients, mentally challenged person.
  • Missing or mobile maxillary anterior teeth or fracture /attrition of the incisal edges during the course of treatment.
  • Patients with cleft lip or palate 8.
  • Y-shaped frenum 9.
  • With unacceptable oral hygiene (PI>2, GI>2) 10.
  • Patient undergoing active orthodontic treatment.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate & compare the maxillary labial frenum position from fixed reference to its insertion point before and after frenectomy using conventional and paralleling techniquePreoperatively and 3 months postsurgery
Secondary Outcome Measures
NameTimeMethod
To evaluate & compare the early wound healing score after maxillary labial frenectomy using conventional & paralleling techniquenext day, one week and after one month
To evaluate & compare the pain experience with visual analogue scale after maxillary labial frenectomy using conventional and paralleling techniquetill one week

Trial Locations

Locations (1)

MIDSR Dental hospital

🇮🇳

Latur, MAHARASHTRA, India

MIDSR Dental hospital
🇮🇳Latur, MAHARASHTRA, India
Gauri Ugale
Principal investigator
9130009068
ugalegauri@yahoo.com

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