Comparison of Intralesional Triamcinolone Versus Verapamil for Keloid Treatment
- Conditions
- Keloid Scars
- Interventions
- Registration Number
- NCT06897969
- Lead Sponsor
- Nishtar Medical University
- Brief Summary
This study aims to compare the efficacy of intralesional triamcinolone and verapamil in patients presenting with keloid at our local setting. The results will guide us towards better management of keloids by choosing the more appropriate treatment. Adequate treatment will reduce significant emotional and physical distress in patients. We hypothesized that mean reduction in Vancouver Scar Score is higher in triamcinolone acetonide group compared to verapamil after three months of treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 60
- size of keloid1-5 cm,
- on any site of the body,
- duration less then five years and
- baseline Vancouver scar score of more the or equal to 5
- Pregnant or lactating women,
- family history of keloids,
- acromegaly, and
- congestive cardiac diseases
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Verapamil Treatment Verapamil Injection One ml (2.5 mg) of Intralesional Verapamil Injection will be administered monthly. The injections will be administered with an insulin syringe of 27-gauge needle. Administration of the treatment medication will be continued till the keloid is flattened or TOTAL DURATION of three months. Triamcinolone Treatment Triamcinolone Acetonide 1 ml of 40 mg/mL suspension Intralesional Triamcinolone acetonide (40mg) will be administered monthly. The injections will be administered with an insulin syringe of 27-gauge needle. Administration of the treatment medication will be continued till the keloid is flattened or TOTAL DURATION of three months.
- Primary Outcome Measures
Name Time Method Change in Vancouver Scar Score Vancouver Scar score will be measured at baseline (before treatment assignment) and then 4-weeks after completion of treatment - 16-weeks after randomization. The Vancouver Scar scale assesses four parameters of vascularity, pigmentation, pliability and height. The total score ranges from 0 - 13.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Nishtar Medical University & Hospital
🇵🇰Multan, Punjab, Pakistan
Nishtar Medical University & Hospital🇵🇰Multan, Punjab, PakistanDr. Asma Batool, MBBSPrincipal Investigator