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Consumer and Eye Irritation Study

A Consumer Insight Study with Instrument-Based Efficacy Assessments and Ocular Irritation (Eye Instillation) Evaluation of a Hydrating Cleanser Without Active Ingredients for Removal of Sunscreen and Everyday Makeup in Healthy Adult Male and Female Participants. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103891
Enrollment
24
Registered
2026-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

None listed

Interventions

Intervention1: Eltior Skin-Reset Cleanser: Marketed By: Relaner Ventures Pvt. Ltd. Route of Application: Topical Mode of Usage: Participants will be instructed to wet the face with water and dispens

Sponsors

Relaner Ventures Pvt. Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Ages 18-55 years both inclusive. 2) Males and non-pregnant/non-lactating females 3) Females with self-reported negative pregnancy test 4) Having general good health and has both eyes. 5) Understand the test procedures and agree to adhere to study requirements, instructions and procedures. 6) Pass an eye sting evaluation using isotonic saline. 7) Willing to refrain from using any eye drops on the day of the study. 8) In general, good health as determined by the Investigator on the basis of medical history. 9) Willig and able to follow the study protocol to participate in the study. 10) Able to understand and provide written Participant s information sheet to participate in the study. 11) Willing not to use any other marketed product on application site during the study period.

Exclusion criteria

Exclusion criteria: 1) Having any known allergy to test product ingredient. 2) Presence of any chronic disease or illness in the past three months or any clinically significant on-going chronic medical illness e.g. Congestive cardiac failure, Hepatitis, Hypotensive episodes, etc. 3) Participation in any similar consumer study within the past 90 days. 4) Currently using any topical medications. 5) Any exceptions to the inclusion/exclusion criteria will be considered on a case-by case basis and will be documented in the case report form. 6) Currently or within the last 2 weeks using eye drops (such as saline solutions, Netra-Prabha, Drasty, etc.). 7) Have participated in a study with the eyes as the target area within 6 weeks of the start of the study. 8) Be involved in any aspect of study administration, i.e., evaluating applying products, etc. 9) Have a history of sensitivity and/or adverse reactions to preparations intended for the eyes. 10) Currently having any eye infections or irritation. 11) The participant is having any sensitivity to eye make-up. 12) Currently have any eye infections or irritation including blepharitis, general lid inflammation, conjunctivitis, or an eye discharge within two weeks of the study. 13) Currently using any topical medications on the face or any medications intended for the eyes. 14) Have taken antihistamines (including those in cold tablets, OTC allergy medications, decongestants and inhalants) on the days of the study. 15) Have any other condition or factor that the Investigator or Ophthalmologist believes may affect the stinging or tearing response or the interpretation of the results. 16) Currently taking any prescription pain medications.

Design outcomes

Primary

MeasureTime frame
To assess the effect of the test product for change in: 1. Skin Hydration 2. Skin overall dryness 3. Consumer Perception Questionnaire 4. Ocular irritation 5.degree of inflammation of bulbar conjunctiva, palpebral conjunctiva, and lacrimationTimepoint: From the baseline before test product usage on Day 01 and after test product usage at T0 (+20) mins on Day 01.

Secondary

MeasureTime frame
NilTimepoint: NA

Countries

India

Contacts

Public ContactMaheshvari Patel

NovoBliss Research Pvt. Ltd.

dr.nayan@novobliss.in07948983895

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026