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Protocol To Evaluate Patient Measurements After Ultrasonic Treatment

NCT01260298 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2011-03-11

No results posted yet for this study

Summary

The objective of this study is to observe body contour changes following treatment using the MC1 device.

Conditions

  • Females Scheduled to be Treated Using the MC1.

Interventions

DEVICE

MC1 Ultrasonic Device

Ultrasonic and zonal massage device.

Sponsors & Collaborators

  • Sound Surgical Technologies, LLC.

    lead INDUSTRY

Principal Investigators

  • Michael Kaminer, MD · SkinCare Physicians

Eligibility

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

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2011-03-31
Completion
2011-03-31

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 NCT01260298 on ClinicalTrials.gov