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Clinical Trials/EUCTR2012-002675-34-NL
EUCTR2012-002675-34-NL
Active, not recruiting
Not Applicable

Surgical and aesthetic outcome, quality of life, and cost-effectiveness of keloid treatment - Keloid

Not provided0 sitesJune 29, 2012
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ConditionsKeloidTherapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17]
DrugsTRIAMCINOLONACETONIDE 40 mg/ml

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Keloid
Sponsor
Not provided
Status
Active, not recruiting
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 29, 2012
End Date
TBD
Last Updated
12 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Not provided

Eligibility Criteria

Inclusion Criteria

  • •Keloid patients, 18\-75 yr old, full mental competence, sufficient knowledge of Dutch or English language, keloid suitable for primairy closure after excision, minimum keloid size of 1x1cm.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range 166
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range 10

Exclusion Criteria

  • •Hypertrofic scars. Keloids less than 1 year existent, burn scars, pregnancy, previous radiotherapy which prohibits additional rediotherapy (only for the group of recurrent keloids), hypersensitivity for lidocaine, adrenaline, triamcinolone. Chronic use (\>1 month) of systemic corticosteroids, or immunosuppressive medication (e.g. TNF alfa inhibitors). Use of systemic chemotherapy. Severe morbidity with a life expectancy of less than one year.

Outcomes

Primary Outcomes

Not specified

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