Skip to content

Human Repeat Use Test of Different Durations

Evaluation of Dermatological Safety of Test Product Retained on Skin of Healthy Human Subjects of Varied Skin Types for Different Durations through Repeat Use Test

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021818
Enrollment
35
Registered
2019-10-30
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: Body wash (Batch No. 109-44): Neat (Retention duration of products on Site 1: 5 min, Site 2: 10 min, Site 3: 15 min and Site 4:30 min) Control Intervention1: Not Applicable: Not Applica

Sponsors

ITC Life Sciences and Technology Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age: 18 to 60 years 2. Subjects in generally good health and not undergoing medical treatment 3. Subjects without any cuts, marks and open wounds or dense hair on both forearms 4. Subjects free of any obvious infection of skin as determined by Dermatologist 5. Subjects willing to give a written informed consent for their voluntary participation in the study 6. Subjects willing to abide by the study requirements and visit the site for regular follow up 7. Subjects willing to refrain from any product ot therapy or cosmetic intervention other that study product on their forearms for a period of one week till study completed

Exclusion criteria

Exclusion criteria: 1 Subjects with known allergies or sensitivities to cosmetic products or its components like fragrances, preservatives etc. 2 Subjects who are currently undergoing or had undergone Dermatological treatments or procedures within the last 1 month. 3 Subjects with pre-existing or dormant Dermatologic conditions (e.g. Psoriasis, Atopic dermatitis, Rashes, Eczema, many and/or severe excoriations etc.) that could interfere with the study outcome as determined by the investigator. 4 Subjects with scars or cuts or wounds or dense hair on forearms which could interfere with assessment. 5 Subjects who are nursing or pregnant (Self declaration or Urine pregnancy test). 6 Subject having participated in any other similar clinical study or test panel within one month prior to enrolment in the current study.

Design outcomes

Primary

MeasureTime frame
1 Dermatologists Visual Assessment of test site for Irritation. 2 Subjectsâ?? Self â?? Assessment of test site for Irritation. 3 Instrumental Measurements- measuring erythema using Mexameter and change in skin colour using Chromameter.Timepoint: Before product application to after 30 minutes of product removal

Secondary

MeasureTime frame
Not ApplicableTimepoint: Not Applicable

Countries

India

Contacts

Public ContactMs Maheshvari Patel

Cliantha Research

nkpatel@cliantha.com9909013286

Outcome results

None listed

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