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Hair fall Benefit Study For The Test Product

To evaluate the efficacy of the test product (Bajaj Hair Oil VCO-08) in hair fall reduction,improving hair growth rate, hair density, and hair thickening in healthy subjects - None

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037100
Enrollment
70
Registered
2021-10-05
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

None listed

Interventions

Intervention1: Bajaj Hair Oil VCO-08: Take approximately 7.5 ml of oil on your palm and apply to one half of the scalp. And take approximately 7.5 ml of oil on your palm the second time and apply to t

Sponsors

Bajaj Consumer Care Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Female subjectsââ?¬• in general good health. 2.Subjects in the age group 18-45 years (both the ages inclusive). 3.Subjects complaining of hair fall and damage. 4.Subjects willing to give a written informed consent and willing to abide by and comply with the study protocol. 5.Hair density of >100 and 6.Female Subjects falling under Grade 3 - Grade 6 of hair loss severity grade evaluated as per photo numerical 10-point scale (Linear scale for assessment purpose-In Use Scale).

Exclusion criteria

Exclusion criteria: 1.Subjects who have undergone hair growth treatment within 3 months before screening into the study. 2.Subjects having any active scalp disease which may interfere in the study ââ?¬â?? dermatologistââ?¬•s judgement. 3.Subjects 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. 4.Subjects who have history of alcoholism, smoking, crash dieting and/ or psychiatric disorder including trichotillomania. 5.Subjects who have had hair transplant, who have taken pharmaceutical product which cause hirsutism (ex. phenytoin) and finesteride for androgenic alopecia, under medical treatment for hair problems. 6.A known history or present condition of allergic response/hypersensitivity to any cosmetic ingredients and pharmaceutical products. 7.Subjects on oral medications, undergoing any chemical hair salon treatment-straightening / perming / colour which will compromise the study. 8.Subjects who are pregnant or lactating or nursing as established with medical history. 9.Menopausal female subjects as determined by medical history. 10.Subjects with chronic illness which may influence the cutaneous state. 11.Subjects participating in other similar cosmetic or therapeutic trial within last three months. 12.Subjects with 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.

Design outcomes

Primary

MeasureTime frame
Significant improvement in hair growth rate, hair density, hair thickness, hair fall with or without bulb, hair fall from the roots, hair and scalp condition, new hair growth.Timepoint: At Day30 & Day60 in comparison to baseline.

Secondary

MeasureTime frame
To evaluate the product safety by dermatologist assessment.Timepoint: At Day30 & Day60 in comparison to baseline.

Countries

India

Contacts

Public ContactDr Mukesh Ramnane

MS Clinical Research Pvt Ltd

mukesh.ramnane@mscr.in08041125934

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026