At a glance
ClinicalIndex Comparison RecordN/ACompleted· 2 enrolled
Drug / intervention
Rotational fractional resection (1.5mm Diameter Device)device
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.
The PREFORM Study: An Exploratory, Single-Center Study to Evaluate the Safety and Efficacy of Rotational Fractional Resection on Submental Contouring and Optimal Peri-Procedure Regimen for Accelerated Recovery
In Brief
A clinical study evaluating Rotational fractional resection (1.5mm Diameter Device) for Skin Laxity and Lipodystrophy. Completed, enrolled 2 participants across 1 site.
Detailed Summary
This study will evaluate the safety and efficacy of rotational fractional resection (RFR) to improve neck contouring. Rotational fractional resection is used to remove loose skin and fat.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSkin Laxity, Lipodystrophy
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
Enrollment StartMar 2019
First PostedMay 2019
Primary CompletionOct 2019
TodayJul 2026
First PostedMay 29, 2019
Enrollment StartMar 20, 2019
Primary CompletionOct 16, 2019
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 7.1 years ago
Interventions
Rotational fractional resection (1.5mm Diameter Device)device
Single treatment of skin resection and with and without focal lipectomy (removal of loose skin and fat)