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Open labelled, single arm, interventional study of hair serum for premature greying of hair

To study efficacy and safety of hair serum containing Greyverse, Euk 134 and Amisol trio in premature greying of hair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041679
Enrollment
10
Registered
2022-04-06
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: L679- Hair color and hair shaft abnormality, unspecified

Interventions

Intervention1: Greyverse, Euk 134 and Amisol trio: Application of the hair serum containing Greyverse, Euk 134 and Amisol trio on the scalp twice daily for 12 weeks, subject aged less than 25 years Co

Sponsors

Apex laboratories private limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged less than 25 years diagnosed with premature canities attending the OPD 2.Patients who are willing to appear for regular follow ups and follow the prescribed treatment regularly. 3.Parents/guardians (legally authorized representative [LAR]) willing to provide written informed consent for patients aged less than 18 years. Patients between 18-25 years of age willing to provide written informed consent

Exclusion criteria

Exclusion criteria: 1.Patients known to be allergic to any of the components of the study medications. 2.History of any chronic systemic disease 3.Patients with known malignancy or those on chemotherapy. 4.Refusal to participate in the study. 5.Participated in a clinical trial in last 90 days

Design outcomes

Primary

MeasureTime frame
To study the efficacy of hair serum containing Greyverse, Euk 134 and Amisol trio in premature greying of hairTimepoint: after 3 months

Secondary

MeasureTime frame
Clinical photographs â?? taken in same position and with uniform illumination. Trichoscopy with video-dermoscope (Fotofinder) before and at the end of study period (Day 0 and 90) to analyse the outcomeTimepoint: after 3 months

Countries

India

Contacts

Public ContactDr Rashmi Agarwal

CUTIS Academy of Cutaneous Sciences

agarwal5rashmi@gmail.com9707778021

Outcome results

None listed

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