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Clinical Trials/CTRI/2019/03/018139
CTRI/2019/03/018139
Completed
Phase 4

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

Ramaiah Indic Specialty ayurveda restoration Hospital0 sites50 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Ramaiah Indic Specialty ayurveda restoration Hospital
Enrollment
50
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 3, 2019
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Ramaiah Indic Specialty ayurveda restoration Hospital

Eligibility 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

  • •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

Outcomes

Primary Outcomes

Not specified

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