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Clinical Trials/CTRI/2014/03/004476
CTRI/2014/03/004476
Completed
N/A

Evaluating Non-Invasive Measurement Tools to Differentiate Cellulite Affected Skin from Normal Skin on Healthy Human Volunteers

ITC R D Centre0 sites10 target enrollmentTBD
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Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
ITC R D Centre
Enrollment
10
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Subjects willing to give written informed consent and abide by the study protocol.
  • •10 healthy female subjects in the age group of 20 to 50 yrs.
  • •At least 5 subjects with cellulite on at least one of the arms/ thighs and the remaining 5 with normal skin.
  • •Subjects with no medical history of disease / medical condition/ concurrent illness/ pre\-existing or dormant dermatologic condition that could interfere with the study results.
  • •Subjects who are not pregnant or nursing.
  • •Subjects who are willing to abstain from using any cosmetic product on the identified sites on the day of study.

Exclusion Criteria

  • •Subjects who are pregnant or lactating.
  • •Subjects having skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations), which would interfere with the test readings.
  • •Subjects on medications (e.g. steroids or antihistamines), which could compromise the study results.
  • •Subjects with scars, cuts/ wounds/ scratches on the potential test sites (Brachium region, Femoral regions and Volar forearm), which could interfere with the test readings.

Outcomes

Primary Outcomes

Not specified

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