Body Fat Disorder Clinical Trial
Official title:
Retrospective Study of Patient Surveys of MMS Experience
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Status | Withdrawn |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 |
Verified date | December 2019 |
Source | Zeltiq Aesthetics |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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
Status | Withdrawn |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. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Zeltiq Aesthetics |
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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