None listed
Conditions
Interventions
Sponsors
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
| Measure | Time 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
| Measure | Time frame |
|---|---|
| NilTimepoint: Nil | — |
Countries
India
Contacts
Dr. Reddys Laboratories Ltd.