Clinical study on Anti-Hair Fall Herbal Shampoo

A prospective, open-label, single arm study to evaluate the efficacy of LAFZ ETHNIC Bhringaraj & Amla Strengthening Anti-Hair Fall Herbal Shampoo in reducing the hair fall in healthy male or female volunteers

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/12/048268

Enrollment

Registered

2022-12-19

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: LAFZ ETHNIC Bhringaraj & Amla Strengthening Anti-Hair Fall Herbal Shampoo: Dosage form: Liquid, Usage: Wet your hair. Take a coin-sized dollop of shampoo and work it into a lather. Gent

Eligibility

Inclusion criteria

Inclusion criteria: 1. Willing to give informed consent. 2. Healthy Indian male/female volunteer aged between 18-55 years (both inclusive) 3. Must be able to adhere to the study visit schedule and other protocol requirements. 4. Willing to complete the questionnaires. 5. Subjects experiencing mild to moderate hair loss. 6. Willing to avoid usage of his/her own hair oils, shampoo and other hair products for at least one week before commencement and during this study.

Exclusion criteria

Exclusion criteria: 1. Pregnancy or breast feeding. 2. Inability to provide voluntary consent. 3. Patients with pre-existing severe systemic disease necessitating long-term medication. 4. Evidence of significant uncontrolled co-morbid disease which in the investigators opinion would jeopardize patient participation. 5. History of cancer, including solid tumours, hematologic malignancies and carcinoma in situ 6. On any medication or supplement for hair loss including finasteride, any other 5-alpha- reeducate inhibitors, minoxidil, steroids or hormonal products during the 3 months prior to study commencement. 7. On any medication or supplement against dandruff including ketoconazole, Selenium sulfide, Salicylic acid, Pyrithione zinc etc during the 3 months prior to study commencement. 8. History of hypersensitivity reactions. 9. Recently undergone hair transplant surgery. 10. Use of any anti-psychotic drugs for one week prior to Baseline. 11. Use of any investigational medication within 4 weeks prior to start of study drug.

Design outcomes

Primary

Measure	Time frame
â?¢% Change in the average decrease in hair fall (tested through 60 second hair comb test, hair pull test) from baseline to last visitTimepoint: Day 0 to Day 45	—

Secondary

Measure	Time frame
To evaluate consumer acceptance as well as their response toward the product through a feedback questionnaire.Timepoint: Day 0 to Day 45	—

Countries

India

Contacts

Public ContactDr Ashok Godavarthi

Radiant Research Services Pvt. Ltd

ashok@radiantresearch.in9880999297

Outcome results