MedPath

Comparison of Intralesional Triamcinolone Versus Verapamil for Keloid Treatment

Phase 4
Not yet recruiting
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
Inclusion Criteria
  • 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
Exclusion Criteria
  • Pregnant or lactating women,
  • family history of keloids,
  • acromegaly, and
  • congestive cardiac diseases

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Verapamil TreatmentVerapamil InjectionOne 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 TreatmentTriamcinolone Acetonide 1 ml of 40 mg/mL suspensionIntralesional 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
NameTimeMethod
Change in Vancouver Scar ScoreVancouver 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
NameTimeMethod

Trial Locations

Locations (1)

Nishtar Medical University & Hospital

🇵🇰

Multan, Punjab, Pakistan

Nishtar Medical University & Hospital
🇵🇰Multan, Punjab, Pakistan
Dr. Asma Batool, MBBS
Principal Investigator

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