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Efficacy check of Tatshan After Sun recovery Gel for sunburn

A Clinical Study to Evaluate the Efficacy of Tatshan After Sun recovery Gel in Reducing Erythma and Inflammation after UV-B Exposure on skin - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/074783
Enrollment
32
Registered
2024-10-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

None listed

Interventions

Intervention1: Tatshan Aftersun Recovery Gel: Approx 0.25gm gel to be applied on one of the irradiated skin patch 1. Route of administration: Topical Frequency: Twice a day Duration: 7 days Control In

Sponsors

Mohb Growell Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Having apparently healthy skin on test area, for whom the investigator considers that the compliance will be correct and who can allow irradiation slightly more than the MED. 2. Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures. 4. Having signed a Consent form. 5. Should be able to read and write (in English, Hindi or local language). 6. Having valid proof of identity and age.

Exclusion criteria

Exclusion criteria: 1. Pregnant or nursing mothers 2.Scars, excessive terminal hair or tattoo on the studied area 3.Henna tattoo anywhere on the body (in case of studies involving hair dyes) 4.Dermatological infection or pathology on the level of studied area 5.Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye) 6.Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures 7.Chronic illness which may influence the outcome of the study 8.Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month) 9.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.

Design outcomes

Primary

MeasureTime frame
Change in Erythema with MexameterTimepoint: Day 2, Day 7

Secondary

MeasureTime frame
Change in Edema by DermatTimepoint: Day 2, Day 7;Change in redness with colorimeterTimepoint: Day 2, Day 7;Change in skin TemperatureTimepoint: Day 2, Day 7

Countries

India

Contacts

Public ContactDr Priya Ramanathan

MOHB GROWELL PRIVATE LIMITED

mohbgrowellchennai@gmail.com9444403001

Outcome results

None listed

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