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Efficacy evaluation of hair tonic in healthy human subjects

A double blinded, randomized, placebo controlled study to evaluate the efficacy of hair tonic on healthy human subjects. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012284
Enrollment
100
Registered
2018-03-01
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: Hair tonic: Dose: 7 ml of hair tonic per day Frequency: daily once Duration: 108 days for each subject. Mode of administration: Topical application Control Intervention1: Placebo: Dose:

Sponsors

ITC R D Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Female subjects falling under Grade 2 â?? Grade-4 of hair loss severity grade 2)Male subjects falling under Grade 2 to Grade 4 of hair loss severity grade

Exclusion criteria

Exclusion criteria: 1)Subjects who are undergoing hair growth treatment 3 months before screening into the study. 2)Subjects who have scalp conditions such as folliculitis, seborrheoic psoriasis of scalp, seborrheoic dermatitis and lichen planopilaris at the time of screening.

Design outcomes

Primary

MeasureTime frame
evaluate the safety and efficacy of the investigational product in hair fall control or growth in comparison to baseline and placeboTimepoint: 1)Dermatological assessment of hair and scalp will be done on visits 1, 2, 4, 6, 8, 10, 12 and visit 14.—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr Mukesh Ramnane

MS Clinical Research Pvt.Ltd.

mukesh.ramnane@mscr.in08040917253

Outcome results

None listed

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