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Intralesional Treatment of Keloids

S

Sohag University

Status and phase

Enrolling
Phase 3

Conditions

Scar, Hypertrophic

Treatments

Drug: Injection

Study type

Interventional

Funder types

Other

Identifiers

NCT06729840
Soh-Med--24-11-05MS

Details and patient eligibility

About

Intralesional injection in treatment of keloid

Full description

Our study will include 45 patient diveded into three groups , follow up will done before each session , 3month after the last session using photographing assessment , scoring , dermoscope

Enrollment

45 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Both sex aged 18-60 having keloid

Exclusion criteria

  • pregnancy , lactation Skin disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

45 participants in 3 patient groups

Group 1
Active Comparator group
Description:
Will include 15 patients will injected with vitamin D
Treatment:
Drug: Injection
Group 2
Active Comparator group
Description:
Will include 15 patients will injected with botulinum toxin type A
Treatment:
Drug: Injection
Group 3
Active Comparator group
Description:
Will include 15 patients will injected with triamcinolone acetonide
Treatment:
Drug: Injection

Trial contacts and locations

1

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Central trial contact

sama alaa, resident doctor

Data sourced from clinicaltrials.gov

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