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A study to check the efficacy of a Traya regime in reducing or managing hair fall.

A randomized, single-blinded, parallel, controlled clinical study to evaluate the efficacy and safety of a test regime in female subjects with hair fall. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079052
Enrollment
80
Registered
2025-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

Intervention1: Regime comprising Hair growth serum, hair oil, neutraceuticals: Serum: 1 mL of the serum will be applied on the divided sections of the scalp using a graduated dropper per application a

Sponsors

Tatvartha Health Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Female Patients aged 18 to 45years with female pattern hair loss 2.Subjects willing to provide written informed consent, indicating that they thoroughly understand the purpose and procedures required for the study and are willing to participate in the study. 3.Patients willing to undergo shaving of a test area on the scalp and have a mark in the target area. 4.Patient s willingness to maintain same hair length. 5.Patients with blood parameters within the normal range as per blood investigations.

Exclusion criteria

Exclusion criteria: 1.Clinically relevant abnormal physical findings which could interfere with the study; in particular, skin damage such as skin abrasion, actinic keratosis or any abnormal findings in the scalp. 2.Clinically significant dandruff. 3.Active unstable thyroid disease, including subjects on therapy for either hyperthyroidism or hypothyroidism unless their dose of thyroid medication has been stable for at least 3 months (self- declared). 4.Patients who had hair transplant surgery or hair weaving. 5.Patient who had light or laser treatment on the scalp. 6.History or evidence of hair loss other than Androgenetic Alopecia (e.g. due to auto-immune, endocrine, mechanical or infectious process or secondary to a scalp dermatological disorder). 7.Patients with active seborrheic dermatitis. 8.Clinically relevant abnormal laboratory values indicative of physical illness (self-declared).

Design outcomes

Primary

MeasureTime frame
Reduction in hair fall, improvement in hair density and improvement in hair quality as per Dermatological assessment, Trichoscan measurement and comb test when compared to placebo, different time points and baseline.Timepoint: Baseline, Month 2, month 4 and month 6. Each timepoint will have 2 visits.

Secondary

MeasureTime frame
change in hair density by dermatological, Trichoscan evaluations, change in hair thickness, hair growth, hair thinning, hair fall by dermatological, instrumental evaluations.Timepoint: Baseline, month 2, month 4, month 6. Each time point will have 2 visits.

Countries

India

Contacts

Public ContactSudhanthiran S

MS Clinical Research Pvt Ltd

ritambhara@msclinical.com08040917253

Outcome results

None listed

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