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effect of oil control face wash

CLINICAL STUDY TO EVALUATE THE EFFECTIVENESS OF A TEST FACE WASH FOR OILY SKINâ?? - EOCFW

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018139
Enrollment
50
Registered
2019-03-18
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: Oil control face wash: First moisten the face and neck, then apply 1gm of the face wash all over the face and neck, gently working up a lather using circular motion and then wash with l

Sponsors

Ramaiah Indic Specialty ayurveda restoration Hospital
Lead Sponsor
Hindusthan unilever limited
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male and female volunteers, with age 18â??45 years 2.Subjects willing and able to provide informed consent voluntarily 3.with facial oiliness as assessed by Baumann skin oiliness scale (SOS) score of >=13 4.Willing to maintain the investigational product use throughout the study. 5.Subjects who have not undergone any skin therapy in last 3 months 6.Subjects with no known allergy to any of the test ingredients 7.Women using oral contraceptives must have been doing so for at least 6 consecutive months prior to entering the study, and are required to continue with the same brand throughout the study period 8.Subjects who are willing to refrain from using any skin care product other than the investigational product, like, moisturizers, face washes and face creams, for the duration of the study 9.Subjects willing and able to comply with all trial requirements 10. Laboratory workup within normal limits; including complete hemogram, glucose, blood urea nitrogen, creatinine, liver function test, lipid profile, thyroid-stimulating hormone, urine pregnancy test

Exclusion criteria

Exclusion criteria: 1.Subjects who have skin diseases like psoriasis, atopic dermatitis etc. at the time of screening 2.Subject with chronic systemic illnesses or treatment that can affect skin health eg. Polycystic ovarian disease 3.Subjects on oral medications or suffering from chronic illness which will compromise the study 4.Women who have stopped using oral contraceptives less than three months prior to entering the study 5.Subjects who have participated in a similar investigation in the past four weeks 6.Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Changes in the skin oiliness will be assessed by visual assessment by a senior Ayurveda clinician using a 5-point scaleTimepoint: Changes in the skin oiliness will be assessed by visual assessment by a senior Ayurveda clinician using a 5-point scale

Secondary

MeasureTime frame
Subject will answer the following skin health self-perception questionnaire at baseline and at end of the studyTimepoint: at the end of 30 days from trial

Countries

India

Contacts

Public ContactDr GG Gangadharan

A unit of Gokula Education Foundation

vaidyaggganga@gmail.com9448278900

Outcome results

None listed

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