MedPath

A Phase IV, monocentric, clinical trial to evaluate and compare the number of nicks and cuts among three different shaving systems on healthy Indian men.

Phase 4
Completed
Registration Number
CTRI/2011/07/001890
Lead Sponsor
Procter and Gamble
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

Healthy Indian men

Age group of 18 to 45 years

Subjects using double razor with bar soap only for shaving in the past 3 months.

Subject having healthy facial skin.

Subject willing to participate in the study.

Subject willing to abide by and comply with the study protocol.

Subject willing to give his consent for study participation.

Exclusion Criteria

Subject allergic to any shaving gel.

Subjects having visible signs of facial irritation, allergy, sunburn, excessive tanning, or blotchy skin color

Subject suffering from any facial skin diseases like allergic contact dermatitis, tinea faciei or tinea barbae, folliculitis (face), severe acne, rosacea, facial psoriasis or other cutaneous manifestations which could interfere with the study.

Subject participated in any other similar investigation in the past 6 months.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To quantify the number of nicks and cuts experienced while shaving with Gillette Guard Razor and Gillette Shaving Gel compared to different shaving systems.Timepoint: The outcome will be measured after the completion 7 weeks (14 shavings) for each volunteer.
Secondary Outcome Measures
NameTimeMethod
ot applicable.Timepoint: Not applicable.
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