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NOT YET RECRUITING
NCT07096830
NA

Efficacy of Tetrachlorodecaoxide (TCDO) Drops in Chronic Wound Healing

Sponsor: Fazeelat Bibi

View on ClinicalTrials.gov

Summary

This is a single-center, randomized controlled trial evaluating the effectiveness of topical tetrachlorodecaoxide (TCDO) solution in enhancing chronic wound healing. The study will compare standard wound care with and without the addition of topical TCDO drops. Eligible adult participants with chronic wounds of more than six weeks' duration will be randomly assigned to either the intervention or control group. The trial aims to assess the rate of wound healing, time to 50% wound closure, pain reduction measured by the Visual Analog Scale (VAS), and cost-effectiveness.

Official title: Efficacy of Tetrachlorodecaoxide (TCDO) Drops in Chronic Wound Healing: Insights From a Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

66

Start Date

2025-08-30

Completion Date

2026-08-30

Last Updated

2025-08-05

Healthy Volunteers

No

Interventions

DRUG

Topical Tetrachlorodecaoxide (TCDO/Oxoferin)

Topical Tetrachlorodecaoxide (TCDO), a solution with antimicrobial and oxygen-releasing properties, will be applied once daily to the wound bed for 21 consecutive days or until satisfactory healing.

OTHER

Standard Wound Care

Standard wound care includes saline irrigation, wound debridement, antibiotic administration as necessary, and sterile dressing. Provided to all participants.

Locations (1)

Khyber Teaching Hospital, MTI KTH Peshawar

Peshawar, Khyber Pakhtunkhwa, Pakistan