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Clinical Trials/CTRI/2023/02/050053
CTRI/2023/02/050053
Not yet recruiting
未知

Comparative study of efficacy, safety and cost effectiveness of topical Clindamycin 1% - Adapalene 0.1% combination therapy with oral doxycycline versus topical Benzoyl peroxide 2.5% - Adapalene 0.1% combination therapy with oral doxycycline in case of moderate to severe facial acne vulgaris: A prospective, randomised, open label parallel studyâ??.

tamil selvi0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
tamil selvi
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
tamil selvi

Eligibility Criteria

Inclusion Criteria

  • Subjects of either gender.
  • 2\. Subjects of 12 to 30 years of age with moderate to severe facial acne vulgaris having \>\= 19 and \<\=38 score based on global acne grading system.

Exclusion Criteria

  • Patients already on anti\-acne medication(topical or oral) in last one month.
  • 2\. Patients having nodulocystic lesions, acne conglobata, acne fulminans, secondary acne.
  • 3\. Patients unwilling to give written informed consent.
  • 4\. Patients with known hypersensitivity to benzoyl peroxide, clindamycin or adapalene and doxycycline.
  • 5\. Pregnant or lactating women.

Outcomes

Primary Outcomes

Not specified

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