Quantitative Evaluation of Skin Shrinkage Caused by a Non-invasive Tightening Device

NCT00894244 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2021-12-28

Study results available
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Summary

This study is being done to measure the amount of skin shrinkage caused by a non-invasive skin tightening device.

Conditions

  • Healthy

Interventions

DEVICE

Radiofrequency device

One treatment pass on one arm. 2-5 treatment passes on the other

Sponsors & Collaborators

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2009-09-30
Completion
2009-09-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00894244 on ClinicalTrials.gov