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NCT03945422 · ClinicalTrials.gov registry record · NA
The Use of RF in Premature Jowl and Neck Laxity Following Facialplasty
A NA study of Premature Jowl and Neck Laxity Following Facialplasty, sponsored by InMode MD.
- Completed
- Registry status
- NA
- Development phase
- 11
- Enrollment target
- 1
- Study location
NCT03945422 is a NA study of Premature Jowl and Neck Laxity Following Facialplasty that has completed, run by InMode MD. The registered enrollment target is 11 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03945422, a NA study of Premature Jowl and Neck Laxity Following Facialplasty, has completed, sponsored by InMode MD.
- COMPLETED
- Registry status
- NA
- Development phase
- 11 participants
- Enrollment target
- 1
- Study location
Study Summary
Study is to evaluate the efficacy of treatment Radio Frequency in premature jowl and neck laxity following facialplasty
Conditions Studied
Interventions
- DEVICE AccuTite/FaceTite
Study Locations (1)
Illinois
- Chicago Center for Facial Plastics - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2019-04-15 |
| Est. Completion | 2021-01-18 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03945422
The ClinicalTrials.gov registry entry for NCT03945422 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is InMode MD, which has 22 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Premature Jowl and Neck Laxity Following Facialplasty appearing as the primary indexed condition, and to 1 intervention - of which AccuTite/FaceTite is the first listed.
NCT03945422 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT03945422 about?
NCT03945422 is a clinical study titled "The Use of RF in Premature Jowl and Neck Laxity Following Facialplasty". Study is to evaluate the efficacy of treatment Radio Frequency in premature jowl and neck laxity following facialplasty
What is the current status of trial NCT03945422?
This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2019-04-15. Estimated completion is 2021-01-18.
What conditions does trial NCT03945422 study?
This clinical trial studies the following conditions: Premature Jowl and Neck Laxity Following Facialplasty.
What interventions are being tested in trial NCT03945422?
The interventions under investigation include: AccuTite/FaceTite (DEVICE).
Who is sponsoring clinical trial NCT03945422?
This trial is sponsored by InMode MD, which has 22 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03945422 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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