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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04199806
Other study ID # ZA19-004
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date November 22, 2019
Est. completion date June 2020

Study information

Verified date December 2019
Source Zeltiq Aesthetics
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To collect data from Allergan Patient Surveys (patient surveys) and Allergan Patient Information Form (patient information form) to describe:

1. Patient demographics

2. Treatment patterns

3. Patient feedback and overall experience with MMS treatment


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2020
Est. primary completion date June 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 22 Years to 65 Years
Eligibility Inclusion Criteria

- Subject has received MMS treatment in the abdomen and/or buttocks (with CoolTone prototype)

- Subject has completed the Allergan patient survey and information form on MMS experience between July 1, 2019 and December 1, 2019.

Exclusion Criteria

• There are no exclusion criteria for this study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaire review
Review data from questionnaires received about MMS experience.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Zeltiq Aesthetics

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy Endpoint: Overall Experience Questionnaire Evaluation of patient overall experience with MMS treatment as measured by patient survey. Immediately post subjects final treatment.
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