Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
NCT07234994

Comparison of the Effect of Ozonized Gel to That of Photobiomodulation Therapy on Wound Healing Following Surgical Gingivectomy

Led by Mennatullah osama ahmed zaki wahba · Updated on 2026-03-03

48

Participants Needed

1

Research Sites

19 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare the effect of photobiomodulation to ozonized gel on wound healing following gingivectomy procedure on adults. The main questions it aims to answer are: Which treatment modality provides less painful and more efficient wound healing ? What are the patient's feedback on different treatment modalities ? Researchers will compare ozonized gel to photobiomodulation to normal gingivectomy procedure with no interference. Participants will: Receive either ozonized gel or photobiomodualtion treatment following surgical gingivectomy Visit the clinic every 3,7,14 and 28 days for checkups and investigations

CONDITIONS

Official Title

Comparison of the Effect of Ozonized Gel to That of Photobiomodulation Therapy on Wound Healing Following Surgical Gingivectomy

Who Can Participate

Age: 18Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients indicated for surgical gingivectomy
  • Adequate amount of keratinized tissue
  • Age between 18 and 40 years
  • Well-educated patients who can follow post-operative instructions precisely
  • Good oral hygiene with a full mouth O'Leary plaque index of 10% or less and a full mouth Gingival Index of zero
Not Eligible

You will not qualify if you...

  • History of smoking
  • Known systemic diseases that interfere with surgical gingivectomy or wound healing
  • Previous adverse reactions to the study products or similar products
  • Pregnant women

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Dentistry, Alexandria University

Alexandria, Egypt, 5310002

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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