Effect of Topical Active Oxygen Therapy on Surgical Site Wound Healing and Microbial Colonization

Early Phase 1

Active, not recruiting

• Conditions: Patients Scheduled for Any Oral Surgical Flap Procedure That Require Suturing Will Be Included in This Study
• Interventions: Drug: topical oxygen gel

• Registration Number: NCT06705920
• Lead Sponsor: Ain Shams University

Brief Summary

To assess the antibacterial efficiency of oxygenated gel therapy on wound healing and microbiological colonization around surgical sutures

Detailed Description

All the patients who will agree to participate in the study and who will sign the informed consent forms. Computer-generated randomization will be used to randomly divide the surgical sites into two groups. Control group: will receive no treatment. Study group: will receive active oxygen gel around suture. Patients scheduled for any oral surgical flap procedure that require suturing will be included in this study. After flap approximation, the surgical site will be sutured using 5-0 braided sutures. In the study group the gel will be applied over the suture and the patients will be instructed to apply the gel to the wound area and to the suture thread using a cotton swab, three times a day after brushing their teeth. Also, patients will be given instructions regarding their post-surgical care.

Study Timeline

• Status Verified: 2024-11
• Study Start: 2024-11-01
• Study First Submitted: 2024-11-23
• Study First Submitted QC: 2024-11-23
• Last Update Submitted: 2024-11-23
• Study First Posted: 2024-11-26
• Last Update Posted: 2024-11-26
• Primary Completion: 2025-03
• Study Completion: 2025-06

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 44

Inclusion Criteria

• Adult patients in a healthy systemic condition who required comprehensive dental treatment
• Both genders with age group > 18 years old
• Patients should approve to deliver a signature to a written consent after study nature explanation.

Exclusion Criteria

• Patients with severe smoking habits >10 cig \ day
• Pregnant females, decisional impaired individuals and handicapped patients
• Patients having poor oral hygiene or not wanting to carry out oral hygiene measures
• Patients on any medication affecting the soft tissue health (e.g., amlodipine, Cyclosporine A, hydantoin)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
test	topical oxygen gel	patient who will undergo intraoral surgical procedures , will have his wound sutured with the addition of blue m gel twice daily

Primary Outcome Measures

Name	Time	Method
Post operative wound healing.	2 weeks	Wound healing will be recorded in the 1st and 2 weeks postoperatively through Landry Wound Healing Index (LWHI) which evaluates the surgical site based on tissue color, response to touch, the marginality of the incision line, and extent of the area. The rating is from 1 = very poor to 5 = excellent.

Secondary Outcome Measures

Name	Time	Method
Microbiological assessment	2 weeks	The collected samples of suture thread will be immersed in phosphate-buffered saline solution (PBS) immediately after their removal and This sample will be subsequently sent to the microbiology laboratory of the Faculty of Pharmacy of the British university in Egypt. The samples will be shaken vigorously for two minutes to separate the bacteria from the suture thread, and to obtain a homogeneous suspension. serial dilutions in saline will be subsequently prepared. 50 microliters of each dilution will be plated in Petri dishes containing different culture media.The blood agar, mannitol agar, MacConkey agar, and Sabouraud agar plates will be aerobically incubated at 37 °C for 24-48 hours. After incubation, the colony forming units (CFUs) will be counted and the total number of CFUs per milliliter of initial solution will be calculated

Trial Locations

Locations (1)

Faculty of Dentistry; 🇪🇬 Al Sherouk, Cairo, Egypt