Hair Benefit Study For The Test Products

Not Applicable

Completed

• Conditions: Health Condition 1: L219- Seborrheic dermatitis, unspecified

• Registration Number: CTRI/2023/02/049737
• Lead Sponsor: nilever Industries Pvt Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-08-07
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 346

Inclusion Criteria

1. Female and male participants in the ratio of 2:1 in general good health.

2. Participants in the age group 18-45 years (both the ages inclusive).

3. Participants willing to give a written informed consent and agree to come for a regular follow up visit.

4. Participants with mild dandruff score of = 40 (adherent (ASFS) + non-adherent dandruff (non-ASFS))

5. Participants willing to abide by and comply with the study protocol.

6. Participants who have not participated in a similar investigation in the past three months.

7. Participants who agree to refrain from using hair dye / hair colour /henna during the study period.

8. Participants willing to refrain from any type of hair treatment like perming, straightening etc. during the study duration

9. Participants willing to refrain from any other anti-dandruff treatment/ products (including lotions/ home remedies/ oils/ serum/ mask) during the course of the study

10. Participants who agree to use test product & regimen (including hair oils).

Exclusion Criteria

1. Participants who have undergone hair growth treatment within 3 months before screening into the study.

2. Participants having any active scalp disease which may interfere in the study – dermatologist’s judgement.

3. Participants with medicated / antidandruff oil will be excluded

4. Participants (male) having androgenic alopecia, male pattern baldness’ not be included in study.

5. Participants who have taken chemotherapy for cancer in the 6 months prior to start of the study or have a plan to do treatments during study.

6. Participants (females) who are pregnant or lactating

7. Participants who have had hair transplant.

8. A known history or present condition of allergic response/hypersensitivity to any cosmetic ingredients and pharmaceutical products.

9. Chronic illness which may influence the cutaneous state.

10. Participants participating in other similar cosmetic or therapeutic trial within last three months

11. Any history of underlying uncontrolled medical illness including diabetes mellitus, hypertension, HIV, hepatitis, severe anemia, serious disorder of heart and respiratory apparatus or any other serious medical illness.

12. Participants (males) who are having androgenic alopecia, male pattern baldness

Study & Design

• Study Type: Interventional
• Study Design: Not specified