Multiple use test to evaluate the skin benefits of ayurvedic products

Completed

• Conditions: Prabhahani/Rukshatha

• Registration Number: CTRI/2021/08/035784
• Lead Sponsor: Unilever Industries Pvt Ltd

Brief Summary

Study will be conducted to assess theefficacy of test product in imparting skin benefits. After consenting andqualifying the inclusion and exclusion criteria subjects will be enrolled intothe study. Post wash out period, Products under test will be randomized andapplications will be done on fore arm. Expert and instrument assessment  will be done during  all the treatment days.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-08-23
• Study Completion: 2021-09-24
• Last Update Posted: 2022-07-02

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 55

Inclusion Criteria

• 1.Healthy male and female subjects between 18-45 years of age.
• 2.Subjects with dry skin as per instrument assessment 3.Subjects with sufficiently long and broad forearms to accommodate the test sites 4.Subjects with uniform skin tone on volar forearm 5.Subjects who have not participated in any clinical product evaluation test in the past 1 month 6.Subjects willing to give a voluntary written informed consent for activities in the study for imaging and agree to come for regular study visits 7.Subjects willing to abide and comply with the study protocol 8.Subjects who are willing not to participate in any other clinical study during participation in the current study.
• 9.Subjects free of excessive hair, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the forearm.
• 10.Subjects who agree not to use of any other product/treatment/soap bar on their forearm during the study period other than product provided 11.Subjects who agree not to carry out bleaching or any other procedures on forearm during the study period.

Exclusion Criteria

• 1.A known history or present condition of allergic response to any sunscreen products, cosmetics products, bathing soaps, detergent powder or medicine 2.Subjects with visible photo-damage on their forearms 3.Subjects having active skin diseases which will interfere with assessments 4.Subjects on oral and topical medications which will compromise the study.
• 5.Suffering from autoimmune diseases like thyroid autoimmunity or diabetes mellitus.
• 6.Subjects who are pregnant, lactating or nursing.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Dermatologist assessment on different skin parameters	Baseline and Post treatment

Secondary Outcome Measures

Name	Time	Method
Instrument assessment of different skin parameters	Baseline and Post treatment

Trial Locations

Locations (1)

MS Clinical Research Pvt. Ltd.; 🇮🇳 Bangalore, KARNATAKA, India

MS Clinical Research Pvt. Ltd.

🇮🇳Bangalore, KARNATAKA, India

Dr Mukesh Ramnane

Principal investigator

08041125934

mukesh.ramnane@mscr.in