Health Condition 1: L91- Hypertrophic disorders of skin
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients with keloids Patients who are willing to participate in the study
Exclusion criteria
Exclusion criteria: Patients below 18 years and above 60 years Pregnancy & Lactation Patient with comorbidities Immunocompromised patients History of previous treatment for keloids and infected ,ulcerated keloids Patients allergic to triamcinolone acetonide , 5-fluorouracil ,and lignocaine Patient not willing to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PIGMENTATION: 0 - Normal 1 - Hypopigmentation 2 - Mixed 3 - Hyperpigmentation PLIABILITY: 0 - Normal 1 - Supple (flexible with minimal resistance) 2 - Yielding (giving way to pressure) 3 - Firm (inflexible, resistant to manual pressure) 4 - Banding (rope like tissue that blanches) 5 - Contracture (permanent shortening of scar producing deformity) HEIGHT: 0 - Normal 1 - Less than2mm 2 - 2 to 5 mm 3 - more than 5mmTimepoint: every 3 weeks for 18 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Treatment side effectsTimepoint: every 3 weeks for 18 weeks | — |
Countries
India
Contacts
Vinayaka Missions Medical College