CTRI/2018/06/014444
Completed
Phase 4
A Prospective study to evaluate the Safety and Efficacy of Investigational Anti-Hair fall shampoo in comparison with Comparator Anti-Hair fall shampoo in subjects with very less to severe Hair fall
Dhathri Ayurveda Pvt Ltd0 sites40 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Dhathri Ayurveda Pvt Ltd
- Enrollment
- 40
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Willingness to give written informed consent
- •Subjects in the range of 18\-50 years of age
- •Subjects with very less to severe Hair fall.
- •Willingness to discontinue any hair care product other than the IP throughout the study.
- •Subjects who are not willing to color their hair throughout the treatment period
- •Subjects willing to stop all the hair treatment such as hair spa, straightening, curling, perming, etc.
- •Subjects with no skin allergies to any cosmetic products
- •Willingness to follow the protocol requirements as evidenced by written informed consent
- •Comprehension of the nature and purpose of the study and compliance with the requirement of the entire procedure
- •In addition, female subjects selected for the study must be able to use a medically acceptable form of birth control during the study or be surgically sterile or be post\-menopausal for at least 1 year.
Exclusion Criteria
- •1\. Subjects with known hypersensitivity to any specific
- •ingredients of IPs
- •2\. Subjects below the age of 18 years and subjects above 50
- •3\. Subjects not willing to participate in the study
- •4\. Subjects who have previously undergone hair transplantation
- •5\. Subjects with any skin diseases.
- •6\. Subjects are being treated for hair fall or severe active
- •infection of any type previously
- •7\. Presence of any underlying significant uncontrolled medical
- •illness involving the cardiovascular, respiratory, renal,
Outcomes
Primary Outcomes
Not specified
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