At a glance
ClinicalIndex Comparison RecordN/ACompleted· 120 enrolled
Drug / intervention
CoolSculpting® Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
International CoolSculpting: Prospective, Multi-Country, Study to Evaluate Patient Satisfaction for Non-Invasive Fat Reduction in Abdomen and/or Flanks (iCOOL)
In Brief
A clinical study evaluating CoolSculpting® System for Non-invasive Fat Reduction. Completed, enrolled 120 participants across 7 sites in 4 countries.
Detailed Summary
This study aims to generate data that conveys participant's experiences such as their overall satisfaction with the CoolSculpting® treatment for their belly and love handles. By doing this, the study will provide insights for doctors to better inform participants about the expected outcomes.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNon-invasive Fat Reduction
CountriesAustralia, Canada, Singapore, United Kingdom
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedApr 2019
Enrollment StartJul 2019
Primary CompletionFeb 2020
TodayJul 2026
First PostedApr 9, 2019
Enrollment StartJul 29, 2019
Primary CompletionFeb 28, 2020
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 7.2 years ago
Interventions
CoolSculpting® Systemdevice
A treatment session is comprised of timed segments of cooling (treatment cycles) followed by 2 minutes of manual massage.