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Keloid Scarring: Treatment and Pathophysiology

Keloid Scarring:A Randomized Clinical and Laboratory Based Study on the Treatment and Differentiation Factors of the Local Disease

Status
Withdrawn
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01295099
Enrollment
0
Registered
2011-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Keloid Scar

Keywords

scar formation, 5-FU, genetic link, psychological impact, social impact

Brief 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

Interventions

5mg of 5FU injected per 1cm square, at 6 week intervals for 30 weeks = 6 sessions

RADIATIONradiotherapy

after complete excision of keloid they have a single session of radiotherapy

DRUGTriamcinolone

TAC 10mg in 1ml injected intralesional

Sponsors

Queen Mary University of London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Keloid Scar Reduction18 monthsUsing a 3D scanner to observe the reduction of the scar volume measured in cubic centimetres

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026