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Clinical Trials/CTRI/2015/11/006363
CTRI/2015/11/006363
Completed
Phase 3

A Randomised Comparative Study of Topical Calcipotriol (0.005%) Vs Topical Calcipotriol (0.005%) along with NBUVB Phototherapy in Patients of Alopecia Areata

DEPARTMENT OF SKIN AND VD0 sites60 target enrollmentTBD
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ConditionsHealth Condition 1: null- PATIENTS OF ALOPECIA AREATA WITH GOOD GENERAL CONDITION AND FREE FROM ANY MAJOR SYSTEMIC ILLNESS.

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: null- PATIENTS OF ALOPECIA AREATA WITH GOOD GENERAL CONDITION AND FREE FROM ANY MAJOR SYSTEMIC ILLNESS.
Sponsor
DEPARTMENT OF SKIN AND VD
Enrollment
60
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
DEPARTMENT OF SKIN AND VD

Eligibility Criteria

Inclusion Criteria

  • •Patients of any age \> 5 yrs, showing features of alopecia areata
  • •\- Patients with a diagnosis of patch type alopecia areata or alopecia totalis
  • •\- No evidence of regrowth present at baseline.
  • •\- Patient should be free from other modalities of treatment atleast for two weeks.

Exclusion Criteria

  • •\- Patients with a history of or active skin disease on the scalp such as psoriasis or seborrheic dermatitis.
  • •\- Patients in whom the diagnosis of alopecia areata is in question.
  • •\- Patients with active medical conditions and other comorbid conditions like infection, eczematization that in the opinion of the investigator would alter the outcome of study evaluation.
  • •\- Patients with history or evidence of hematopoietic abnormality
  • •\- Patients with history or evidence of renal or hepatic impairment.
  • •\- Patients with history of immunosuppression or history of recurrent serious infections.
  • •\- History of photodermatitis or photosensitivity
  • •\- Patients taking oral corticosteroids or applying topical corticosteroids or treatment from outside.
  • •\- Patients with allergy to any component of calcipotriol preparation

Outcomes

Primary Outcomes

Not specified

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