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Protocol To Evaluate Patient Measurements After Ultrasonic Treatment

NCT01373827 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2012-03-26

No results posted yet for this study

Summary

Patients enrolled in this study will come from the Investigator's patient population and be ordinarily suitable for treatment using the MC1 device. The treatment they receive will be no different if they participate than if they do not. The study is only to observe the patients before, during and after their usual treatment.

Conditions

  • Patients Treated With VaserShape MC1

Interventions

DEVICE

VASERShape MC1

Use of the VASERShape MC1 device as part of routine practice

Sponsors & Collaborators

  • Sound Surgical Technologies, LLC.

    lead INDUSTRY

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2012-03-31
Completion
2012-03-31

Countries

  • United States

Study Locations

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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 NCT01373827 on ClinicalTrials.gov