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An observational study to assess clinical impact of hair serum in Indian Patients with patterned hair loss

An Investigator Initiated Observational study to assess the Safety & Clinical impact of Curcumin longa based Hair Serum in Indian Patients with AGA & FPHL (SCALP Study) - NA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/07/055158
Enrollment
120
Registered
2023-07-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: L649- Androgenic alopecia, unspecified

Interventions

Intervention1: Cuticapil Stem Hair Serum: 2% Minoxidil Monotherapy or with 2% Minoxidil therapy and Cuticapil Stem (Purmed water, caffeine, herbasome, Zemea propandiol, procapil, DC 193 C, Capilia Lon

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Male or female patients of 18 or above with diagnosis of hair loss Hair shedding > 6 month Clinical diagnosis of male AGA Grade III, Grade IV, Grade V and clinical diagnosis of FPHL Grade II and Grade III naïve cases or treated with 5% Minoxidil. Patients with no known allergy. Patients who agree to refrain from using hair dye, oil treatment or spa treatment, perming or straightening during the treatment/observation period Patients who agree to use Non ketoconazole based shampoo

Exclusion criteria

Exclusion criteria: Cosmetic hair treatments 1 month prior to enrolment Patients with Hemoglobin level below 10.5 Patients with thyroid disorders or other systemic disorders including T2DM, Hypertension, HIV, Hepatitis, Anemia, Heart disorders, Cancer & undergone chemotherapy, Depression, any psychiatric disorders and those taking drugs which could cause alopecia Pregnant and lactating females Patients with scalp disease Heavy Smokers & heavy drinkers Patients on crash diets

Design outcomes

Primary

MeasureTime frame
Change in hair count shedding after shampooing from baseline at 10 weeks. Change in hair count with Pull test from baseline at 10 weeks. Global photography assessment at 10 week as centrally adjudicated scale score for hair count.Timepoint: at 10 week

Secondary

MeasureTime frame
Safety assessment of the hair serum AGA, FPHL, Patient Global Assessment Timepoint: At 10 week

Countries

India

Contacts

Public ContactDr Rathish Nair PhD MBA

Torrent Pharmaceuticals Ltd

krishnaprasadkorukonda@torrentpharma.com7069000572

Outcome results

None listed

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