Retrospective Study of Patient Surveys

Retrospective Study of Patient Surveys of MMS Experience

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04199806

Enrollment

Registered

2019-12-16

Start date

2019-11-22

Completion date

2020-06-30

Last updated

2019-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Body Fat Disorder

Brief 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

Interventions

OTHERQuestionnaire review

Review data from questionnaires received about MMS experience.

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

OTHER

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

22 Years to 65 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026