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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03090048
Other study ID # Tawar -1
Secondary ID
Status Not yet recruiting
Phase Early Phase 1
First received
Last updated
Start date April 1, 2021
Est. completion date October 31, 2021

Study information

Verified date February 2021
Source Manchanda Medical Clinic
Contact Vinod C Tawar, M.Sc., M.D.
Phone 604 754 2235
Email Tawar.vinod@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients seen with acne lesions not having responded to existing treatments will be offered a placebo or a topical preparation consisting of Vitamin A USP with or without Azithromycin for a duration of 4-6 months USP for the objective of resolving the lesions without systemic side effects and via weekly follow-ups.


Description:

The concentrations of the active ingredients is based on the enclosed articles and the formulations have been modified with an objective of minimizing the side effects.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date October 31, 2021
Est. primary completion date August 24, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 45 Years
Eligibility Inclusion Criteria: - Patients with active lesions Exclusion Criteria: - Patients on a treatment - Asymptomatic patients

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Vitamin A
Vitamin A 2-3 % concentration
Azithromycin
azithromycin monohydrate

Locations

Country Name City State
Canada Manchanda Mc Surrey British Columbia

Sponsors (1)

Lead Sponsor Collaborator
Manchanda Medical Clinic

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Bartlett KB, Davis SA, Feldman SR. Tolerability of topical antimicrobials in treatment of acne vulgaris. J Drugs Dermatol. 2014 Jun;13(6):658-62. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement (dimensions) of acne lesions follow-up focussed on observation of changes Every 4 weeks up to16 weeks
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