Evaluation Anti dandruff effect of the test product

A clinical study to evaluate the Anti dandruff efficacy of test product. - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/02/079940

Enrollment

Registered

2025-02-04

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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

Conditions

None listed

Interventions

Intervention1: Scalp product: The product is applied on whole scalp with the frequency of 3 times in a week for the period of 4 weeks. Control Intervention1: Nil: NA

Eligibility

Inclusion criteria

Inclusion criteria: 1)Healthy male & female volunteers between 18-45 years of age. 2)Volunteer presenting with dandruff as per dermat assessment 3)Volunteer in good health condition as per the medical screening criteria with no disease state or physical condition that the Investigator believes could interfere with the interpretation of the data. 4)Volunteer able to read, understand and sign an appropriate informed consent form indicating her willingness to participate. 5)Volunteers agreeing to comply with following study restrictions: - Volunteers Willing to refrain from application of any other product/treatment on their scalp and hair shafts during the study period. - Not applying any cosmetic, hair care product, test product and/or water 48 hours before scheduled visits.

Exclusion criteria

Exclusion criteria: 1)Volunteers who participated in a study with scalp/ hair shaft as the target area within 4 weeks of the start of this study or is currently participating in such a study. 2)Volunteer pregnant or planning to become pregnant. 3)Volunteers who are breastfeeding or having stopped to breastfeed in the past three months. 4)Volunteers with any other signs of significant local irritation, erythema or skin disease on scalp as well as on the visible parts of the body skin site. 5)Volunteers with self-perceived sensitive skin. 6)Volunteers having chronic illness or had major surgery in the last year. 7)Volunteers undergoing any treatment of any skin condition on body

Design outcomes

Primary

Measure	Time frame
Significant reduction in dandruff flakesTimepoint: Baseline, 1 week, 2 week, 3 weeks, 4 week and 5 weeks	—

Secondary

Measure	Time frame
Reduction in scalp itchTimepoint: Baseline, 1 week, 2 week, 3 weeks, 4 week and 5 weeks	—

Countries

India

Contacts

Public ContactDr Mohit Lalvani

MASCOT-SPINCONTROL India Pvt. Ltd.

poojayadav@mascotspincontrol.in02243349191

Outcome results