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To study the effect of Atarax cream in human volunteers with itching.

A monocentric, single group study to evaluate the effect of Atarax cream in participants with pruritis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040739
Enrollment
31
Registered
2022-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

None listed

Interventions

Intervention1: Atarax cream: Sufficient quantity of product to be applied on areas where itching is experienced by gentle rubbing. Control Intervention1: Nil: Nil

Sponsors

Dr Reddys Laboratories Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Men and women between 18 and 55 years of age. (inclusive) diagnosed with chronic pruritus with dryness 2. Participants with Chronic itch for more than 6 weeks (H/o Itch everyday ) 3. Itch score on Visual analog scale (VAS) (mild to moderate ââ?¬â?? equal to or less than 7 on VAS), on at least 1 site, , 4. Cooperating to comply with protocol procedures and treatments, after being informed of the need and duration of the examinations/treatments.

Exclusion criteria

Exclusion criteria: 1.Pregnant women as confirmed by UPT 2. Females of childbearing potential who are unable or unwilling to use adequate contraception or who are breast feeding 3. Participants with serious skin conditions like psoriasis, Uraemic pruritus 4. Participants Having known allergy to active ingredient or to any cosmetic. 5. Presence of any medical condition or disability that could interfere with study 6. Participants with Any systemic/topical treatment for itching for considerable duration.

Design outcomes

Primary

MeasureTime frame
1. Patient questionnaire response will be taken, based on 10-point VAS. 2. Time point at which they need to reapply (Itch free period) will be recorded.Timepoint: Baseline, 3 mins, 5 mins, 10 mins, 15 mins, 30 mins, 60 mins, 90 mins, 2 hrs, 4 hrs, 6 hrs, 8 hrs post application of test product.

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactRoheet Mohan Rathod

Dr. Reddys Laboratories Ltd.

roheet.mohanr@drreddys.com9561733556

Outcome results

None listed

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