Health Condition 1: L659- Nonscarring hair loss, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: i. Healthy Indian male/female volnteer aged between 18-65 years (both inclusive) ii. Willing to give Informed Consent iii. Subjects with the complaints of mild to moderate hair fall. iv. Willing to complete the study assessments/questionnaires. v. Willing to avoid usage of his/her own hair oils and other hair products for at least one week before the commencement and during this study.
Exclusion criteria
Exclusion criteria: i. Pregnancy or breast feeding. ii. Patients with pre existing severe systemic disease necessitating long term medication. iii. Evidence of significant uncontrolled co morbid disease which in the investigators opinion would jeopardize patient participation. iv. History of cancer, including solid tumors, hematologic malignancies and carcinoma in situ v. Any neurological congenital or acquired, vascular or systemic disorder which could affect any of the efficacy assessments. vi. Participation in the current or previous clinical trial with any approved or investigational products during the past 1 month
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| a)% Change in the average decrease in hair fall (tested through 60 second hair comb test) from baseline to last visit. b)% Change in the average decrease in hair fall through Hair-shedding Visual scale. c)Consumer feedback will be obtained via a set of subjective questionnaires to evaluate the response towards the product Timepoint: Day 0 to Day 42 | — |
Secondary
| Measure | Time frame |
|---|---|
| i. Hair-shedding Visual scale ii. 60 Second hair comb test iii. Feedback questionnaires iv. Collection of unused IPâ??s v. Concomitant Medication Timepoint: Day 0 to Day 42 | — |
Countries
India
Contacts
Radiant research services pvt. Ltd