Skip to main content
Clinical Trials/CTRI/2022/06/043013
CTRI/2022/06/043013
Completed
Phase 2

A Randomized, Prospective, Comparative Clinical Study to evaluate efficacy and safety of NANSHO Hair Oil in mild to moderate Hair loss in females. - NI

amaskar Ayurved Private Limited0 sites71 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: L659- Nonscarring hair loss, unspecified
Sponsor
amaskar Ayurved Private Limited
Enrollment
71
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
September 6, 2022
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
amaskar Ayurved Private Limited

Eligibility Criteria

Inclusion Criteria

  • 1\.Subjects suffering from mild to moderate hair loss (40\-140 Hair by Comb test and Finger Test).
  • 2\.Subjects who are infrequent hair oil users
  • 3\.Subjects who are willing to give informed consent and ready to comply with the protocol
  • 4\.Subjects who are ready to provide regular follow ups till the completion of the study.

Exclusion Criteria

  • 1\.Subjects with severe Hair fall due to any clinically significant disorder/s like anemia, thyroid disorders etc.
  • 2\.Subject with severe dermatological disorders of the scalp that might interfere with the study evaluation
  • 3\.Subjects with recent disease history like, malaria, typhoid, jaundice and scalp diseases and subjects who in the opinion of the investigator are not eligible for enrollment in the clinical study
  • 4\.Subjects who have regularly used anti\-hair fall treatment with hair oils over the last 6 months.
  • 5\.Subjects who have previously undergone hair transplantation procedures
  • 6\.Subjects on systemic steroids for more than 14 days within 2 months prior to enrollment.
  • 7\.Subjects on immunosuppressive drugs
  • 8\.Known cases of Hypersensitivity to hair oil contents
  • 9\.Subjects who have participated in any other clinical study since last 3 months
  • 10\.Subjects who are reported pregnant/planning a pregnancy or lactating.

Outcomes

Primary Outcomes

Not specified

Similar Trials