Overview

Keloid Scarring: Treatment and Pathophysiology

Status:
Unknown status
Trial end date:
2015-01-01
Target enrollment:
0
Participant gender:
All
Summary
To clarify the mechanisms of Keloid scar formation. Elucidate the action and therapeutic value of 5-FU in Keloid scar treatment Identify the genetic link with Keloid scar formation. Quantify the psychological/social impact in keloid scarring patients
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Queen Mary University of London
Treatments:
Fluorouracil
Triamcinolone
Triamcinolone Acetonide
Triamcinolone diacetate
Triamcinolone hexacetonide
Criteria
Inclusion Criteria:

- Adult ( > 18 years old).

- Keloid scarring present.

- Able to understand and give informed consent.

- Patients giving informed consent to donate keloidal or non-affected skin when that is
redundant after a procedure (i.e. BBR, Abdominoplasty).

- Patients with a strong familial pedigree of keloid scar formation.

Exclusion Criteria:

- Open wound at or proximity of the lesion

- Infected lesion

- Pregnant or planning pregnancy in the near future

- Lactating (Breast Feeding)

- Abnormal renal or liver function tests

- Atrophic scars

- Patient under 18 years of age

- Immunocompromised

- OR immunosuppressed