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Clinical Trials/EUCTR2006-005597-43-GB
EUCTR2006-005597-43-GBActive, not recruitingPhase 1

Topical Retinoids and Diabetic Neuropathic Ulceration - Retinoid Study

niversity of Birmingham0 sites40 target enrollmentStarted: September 14, 2007Last updated:

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Enrollment
40

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Inclusion Criteria

  • 1.Type 1 or Type 2 Diabetes as defined by the World Health Organisation classification.
  • 2.Age between 18-70 years.
  • 3.Women of child bearing potential must be using an acceptable method of contraception to prevent pregnancy when they are enrolled in the study and must agree to continue to practice an acceptable method of contraception for the duration of their participation in the study.
  • 4.Must meet the specified criteria for diabetic neuropathy and have no risk factors for other causes of neuropathy
  • 5.Willingness to sign the Centre for Research Ethics Committee (COREC) approved informed consent form.
  • 6.The presence of microalbuminurea and/or retinopathy.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • 1.Nursing mothers, pregnant women (excluded by a negative pregnancy test).
  • 2.Patients with a history of drug or alcohol dependence within the last 5 years.
  • 3.Patients with severe systemic disease other than diabetes which has a recognized complication of neuropathy.
  • 4.Patients with a history of previous kidney, pancreas or cardiac transplantation.
  • 5.Serious or unstable medical or psychological state that may interfere with study participation.
  • 6.Patients having taken part in another investigational drug study within the last three months.
  • 7.Patients who refuse to sign the informed consent form.
  • 8.Patients with pre-existing generalized skin conditions which might affect skin structure or function such as eczema, psoriasis.
  • 9.Patients who are on long term steroid or immunosuppressive therapy.

Investigators

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