None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male and female volunteers 18-50 years old, inclusive. Able to provide informed consent after risks and benefits of the study have been explained. Be willing to undergo all study procedures Ability to communicate effectively with study personnel. Agree to abstain from use of any hair growth affecting oral or topical medication including over the counter and herbal medications, minoxidil, finasteride or dutasteride during the course of this study; also agrees to abstain from shaving the head during the course of the study
Exclusion criteria
Exclusion criteria: Women who are pregnant or lactating. Subjects who took any medicine which can affect the hair growth in recent 3 months. Subjects who have used minoxidil or any oral or topical medication including over the counter and herbal medications for the treatment of hair loss within 6 months of study screening, or finasteride or dutasteride within 12 months of study screening. Subjects with scalp / skin infection, history of hypersensitivity to study products which may interfere in the study. Received any other investigational medicinal therapy within 30 days and topical therapy within 7 days prior to screening Patient suffering from any active general illness or have history of any general illness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the efficacy of kalimera hair oil in the improvement of Hair growth (Trichoscan technique), Hair strength (Universal Tensile Testing Machine (UTM) and Improvement in scalp dandruff (By adherent scalp flaking score).Timepoint: day0 day90 | — |
Secondary
| Measure | Time frame |
|---|---|
| Compare the changes in Manual assessment of hair loss by One min (60sec) comb test or hair count test from screening visits to end of visits. Self-assessment of hair lustrous(shininess) by subjective questionnaires atTimepoint: Day 0 and Day 90 | — |
Countries
India
Contacts
BioAgile Therapeutics Pvt Ltd