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Topical Tacrolimus 0.1% Ointment For Treatment Of Cutaneous Crohn's Disease

This study has been completed.
Information provided by:
University of Aberdeen Identifier:
First received: November 2, 2010
Last updated: NA
Last verified: November 2010
History: No changes posted
An assessment of the efficacy of topical tacrolimus in the treatment of cutaneous crohns disease

Condition Intervention Phase
Crohn Disease Drug: Tacrolimus Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Topical Tacrolimus 0.1% Ointment for Treatment of Cutaneous Crohn's Disease

Resource links provided by NLM:

Further study details as provided by University of Aberdeen:

Primary Outcome Measures:
  • Assessment of standardised digital photography by three independent assessors following the Physicians' Global Severity Scale before and after treatment [ Time Frame: At 12 weeks of treatment, optionally extended to 52 weeks ]

Secondary Outcome Measures:
  • Global Self Assessment [ Time Frame: 12 weeks, optionally extended to 52 weeks ]
  • Perineal Disease Activity Index [ Time Frame: 12 weeks, optionally extended to 52 weeks ]

Enrollment: 20
Arms Assigned Interventions
Experimental: Topical tacrolimus
Once daily topical application
Drug: Tacrolimus
Once daily application for 12 weeks followed by 4 weeks observation. Optional 36 week open label extension
Other Names:
  • Protopic 0.1%
  • FK506


Ages Eligible for Study:   12 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • willingness and capability to follow the study procedure
  • confirmed diagnosis of Crohn's Disease of at least 3 months duration confirmed by radiography, endoscopy or pathological examination
  • required to have a skin manifestation of Crohn's disease
  • required to give written informed consent
  • both male and female subjects with reproductive potential required to be on an acceptable form of birth control for the duration of the study
  • long-standing, concomitant immunosuppressive therapy was allowed if the dose was stable and not controlling the skin problem

Exclusion Criteria:

  • known sensitivity to tacrolimus
  • change in aminosalicylate dosage in the four weeks prior to screening
  • on oral steroids at over 40mg per day
  • been commenced on methotrexate, azathoprine or ciclosporin within the last two months
  • commenced on a a TNF-alpha monoclonal antibody within the three months prior to screening
  • patients having had a stoma fashioned less than three months before enrolment
  • patients with an immunocompromising disease
  • patients with a diagnosis of malignancy within the last five years
  • patients with any other condition, past or present treatment thought by the investigator to render the subject ineligible for the study
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Please refer to this study by its identifier: NCT01233570

United Kingdom
University of Aberdeen, Aberdeen Royal Infirmary
Aberdeen, Grampian, United Kingdom, AB25 2ZN
Sponsors and Collaborators
University of Aberdeen
Principal Investigator: Anthony D Ormerod, MBChB University of Aberdeen
  More Information

Responsible Party: Dr AD Ormerod, University of Aberdeen Identifier: NCT01233570     History of Changes
Other Study ID Numbers: 33000332
Study First Received: November 2, 2010
Last Updated: November 2, 2010

Keywords provided by University of Aberdeen:
Cutaneous Crohns Disease
Topical Tacrolimus
Metastatic Crohns Disease
Pyoderma Gangrenosum
Granulomatous chelitis
Oral crohns disease
Perianal crohns disease

Additional relevant MeSH terms:
Crohn Disease
Inflammatory Bowel Diseases
Gastrointestinal Diseases
Digestive System Diseases
Intestinal Diseases
Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs
Calcineurin Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action processed this record on September 21, 2017