Skip to content

Evaluate effect and safety Of VB-001, an Antidandruff Hair Oil Regime In Comparison With Head & Shoulders® Antidandruff Shampoo (P&G) Regime In Subjects With Moderate Adherent Dandruff Of The Scalp

Efficacy and in use skin safety Of VB-001, an Antidandruff Hair Oil Regime In Comparison With Head & Shoulders® Antidandruff Shampoo (P&G) Regime In Subjects With Moderate Adherent Dandruff Of The Scalp

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/01/003283
Enrollment
168
Registered
2013-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Antidandruff hair oil regime: Antidandruff hair oil (active ingredient Piroctone Olamine) application of 10ml of Product daily, overnight (at least for 8 hours leave on) with massage

Sponsors

Vyome Biosciences Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy males or females aged >= 15 years and 2.Understand and willing to sign written informed consent in case of adults and written parental consent form and child assent form in case of children wherever applicable. 3. Must be willing and able to comply with protocol, including measures of subject compliance. 4. Must have active adherent dandruff of the scalp with a minimum score of 6 and not exceeding 14; baseline scaling scoring of at least 3 and not more than 4 of adherent flaking in at least one zone of the scalp (6 zones- 2 frontal, 2 parietal plus temporal and 2 occipital) . 5. Investigators global assessment (IGA) for pruritis score of at least 1. 6. Should not have used an antidandruff agent in the past 14 days. 7. Willing to refrain from use of all other topical medications that would affect the results of the trial, including medicated shampoos/oils or antibiotics, during the treatment and observation periods (from day 0 to day 14).

Exclusion criteria

Exclusion criteria: 1. Pregnant or Lactating Women by history. 2. No history of overt bacterial, viral or fungal infection of the head/neck. 3. No history or presence of compromising dermatosis elsewhere on the skin. 4. No actinically damaged skin 5. Presence of any skin condition that would interfere with the diagnosis or assessment of adherent dandruff; e.g., psoriasis, acne, atopic dermatitis. 6. Clinically significant systemic disease (e.g., immunological deficiencies, AIDS, current malignancies, uncontrolled diabetes mellitus). 7. Use within 1 month prior to baseline of any treatment that would affect the results of the trial, including 1) systemic antifungals, 2) systemic steroids 3) systemic antibiotics 4) systemic anti-inflammatory agents or 5) cytostatic or immunomodulating drugs (e.g., cyclosporine, tacrolimus, pimecrolimus). 8. Use within 2 weeks prior to baseline of any treatment that would affect the results of the trial, including 1) topical steroids 2) topical retinoids 3) topical anti-inflammatory agents 4)topical antibiotics or 5) topical treatment of adherent dandruff (e.g., coal tar preparations, antidandruff shampoos/oils/gels/creams/conditioners 6) antihistamines.

Design outcomes

Primary

MeasureTime frame
To evaluate efficacy of VB-001, antidandruff hair oil regime in comparison with Head & Shoulders® Antidandruff Shampoo (P&G) regime in subjects with Moderate adherent dandruff of the scalp.Timepoint: 0,5 ,9,and 14 days

Secondary

MeasureTime frame
To evaluate in use skin safety VB-001, antidandruff hair oil regime in comparison with Head & Shoulders® Antidandruff Shampoo (P&G) regime in subjects with Moderate adherent dandruff of the scalpTimepoint: 0,5 ,9,and 14 days

Countries

India

Contacts

Public ContactDr Abhijit Bapat

C.L.A.I.M.S. Pvt. Ltd.

rsjdr@rediffmail.com66758851

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 26, 2026