Efficacy study of the given sample-Hair styling gel

Active, not recruiting

• Conditions: 30 Male healthy human subjects with damaged hair.

• Registration Number: CTRI/2018/05/014155
• Lead Sponsor: Godrej Consumer Products Ltd

Brief Summary

This will be a prospective , open label, one arm efficacy test. This

will be 15 Days study. The subjects will be assessed by the

dermatologist on Visit 1- Screening and application , Visit 2 – next

day , Visit 3 – 7th day , Visit 4 – 14th day.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2018-10-08
• Study Start: 2018-12-05

Recruitment & Eligibility

• Status: Closed to Recruitment of Participants
• Sex: Male
• Target Recruitment: 30

Inclusion Criteria

• Volunteer ( Male ) in generally good health.
• Volunteer between the ages of 18 and 50 years.
• Volunteer has not participated in a similar clinical investigation in the past three months.
• Volunteer willing to give a written informed consent, agrees for audio video consenting procedures and come for regular observation.
• Volunteer having mild to moderate hair damage 6.
• Volunteer with very dry hair.

Exclusion Criteria

• Known history or present condition of allergic response to any cosmetic products.
• Skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations on the scalp), which would interfere with the test readings.
• Medications (e.g. steroids or antihistamines), which would compromise the study.
• Known alcohol or drug abuse.
• Any history of underlying uncontrolled medical illness including diabetes, liver disease or any other serious medical illness 6.
• Volunteers participating in any other cosmetics or any other clinical trial.
• Hypersensitivity to any of the tested products.
• Use of Hormonal Contraceptives either Oral or Implants.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Efficacy evaluation of cosmetic formulation (Hair Styling gel) in conferring wet hold damage control on 30 healthy human subjects.	Visit 1- Screening and application , Visit 2 – next | day , Visit 3 – 7th day , Visit 4 – 14th day.

Secondary Outcome Measures

Name	Time	Method
-	-

Trial Locations

Locations (1)

Kasturmahal Polyclinic; 🇮🇳 (Suburban), MAHARASHTRA, India

Kasturmahal Polyclinic

🇮🇳(Suburban), MAHARASHTRA, India

Dr Sudhir Medhekar

Principal investigator

9820321430

sudhir.medhekar@gmail.com