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24 hours patch test to verify the Primary irritation of a research product

Dermatological assessment of primary irritation of stempeucareâ?¢ using patch test technique on skin of adult healthy human volunteers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/02/004427
Enrollment
24
Registered
2014-02-21
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: STM-1: dose 40 micro liters of skin health serum route of administration-applied topically in the form of patch Frequency - one application duration - patch applied for 24 hours. In

Sponsors

Stempeutics Research Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy male and female subjects in the ration of 1:1. Subjects with skin phototype III to V and Subjects willing to keep the patch in position for 24 hours. Subjects willing to come for follow up visit at specified interval for 9 days. Subjects ready to follow instructions during the study period. Subjects with healthy skin on the studied anatomic unit (free of eczema, wounds and inflammatory scars). Subjects representing varied skin types (representation of all 4 skin types â?? oily, normal, dry and combination).

Exclusion criteria

Exclusion criteria: Subjects having infection, allergy, bruises or scars on the area to be tested. Subjects having known hypersensitivity to any component of the tested products. Subjects having sensitivity to penicillin, based on history or as confirmed by a sensitivity test on forearm. Athletes and subjects with history of excessive sweating. Subjects with cutaneous disease that may influence the study result as per investigatorâ??s judgment. Subjects having chronic illness that may influence the cutaneous state (for example: SLE) as per investigatorâ??s judgment. Subjects on oral corticosteroid therapy. Any history of underlying uncontrolled medical illness (including diabetes, liver disease or history of alcoholism, HIV or any other serious medical illness) which in the investigatorâ??s opinion will have safety concerns for the subject. For females: Being pregnant or breastfeeding or having stopped breastfeeding within the last three months.

Design outcomes

Primary

MeasureTime frame
verification of safety of Investigation product by evaluating the irritation potentialTimepoint: 24hrs 48hrs and 7 days after patch application

Secondary

MeasureTime frame
DrynessTimepoint: 24hrs 48hrs and 7 days after patch application

Countries

India

Contacts

Public ContactShwetha Gautam Mantagani

CIDP Biotech India Pvt Ltd

rnangia@cidp-cro.com01140793385

Outcome results

None listed

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