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NCT06157853 · ClinicalTrials.gov registry record · NA
Evaluating Procedure Pairing of a Post-Procedure Cream Versus a Comparator in Patients Treated With a Radiofrequency Microneedling for Facial Rejuvenation
A NA study of Wrinkle and Photoaging, sponsored by Revision Skincare.
- Completed
- Registry status
- NA
- Development phase
- 11
- Enrollment target
- 1
- Study location
NCT06157853: Completed NA study of Wrinkle and Photoaging, sponsored by Revision Skincare.
NCT06157853 is a NA study of Wrinkle and Photoaging that has completed, run by Revision Skincare. The registered enrollment target is 11 participants, below the 120-participant average among 25 other Wrinkle trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06157853, a NA study of Wrinkle and Photoaging, has completed, sponsored by Revision Skincare.
- COMPLETED
- Registry status
- NA
- Development phase
- 11 participants
- Enrollment target
- 1
- Study location
Study Summary
This randomized, single-center, double-blinded, controlled, clinical trial was conducted to investigate the tolerability, safety, and efficacy of a post-procedure cream when used immediately after radiofrequency microneedling and for seven days post-procedure with twice daily application in healthy female subjects ages 35-65 with moderate facial photodamage (Grade II or III) using the Glogau Scale of Photoaging. Furthermore, this clinical trial will compare the active post-procedure cream to a comparator anhydrous cream product often paired with skin rejuvenation procedures. A total of 11 healthy female subjects completed the study. Six (6) subjects in the active arm and five (5) subjects in the comparator arm.
Primary Outcome
The primary tolerability endpoint will be Investigator Tolerability Assessment of erythema, edema, and dryness. A change in scores or lack of significant change after procedure, immediately post-procedure, post product application, Day 1 (24 hours), Day 3, and Day 7 in comparison to baseline (post-procedure) indicates tolerability / safety of the test material. Four-point scale with a lower score indicating a better outcome. 0 = None 1. = Mild 2. = Moderate 3. = Severe
Conditions Studied
Interventions
- PROCEDURE Radiofrequency Microneedling
- OTHER Facial Cleanser
- OTHER Facial Moisturizer
- OTHER Sunscreen
Study Locations (1)
Tennessee
- Tennessee Clinical Research Center - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2022-07-11 |
| Est. Completion | 2022-08-23 |
| Phase | NA |
What the finished NCT06157853 record still lists
NCT06157853 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 120-participant average among 25 other Wrinkle trials with a reported enrollment target (91% lower).
The record links to 2 conditions, with Wrinkle appearing as the primary indexed condition, and to 4 interventions - of which Radiofrequency Microneedling is the first listed.
NCT06157853 reports a single indexed study location in Tennessee.
Frequently Asked Questions
What is clinical trial NCT06157853 about?
NCT06157853 is a clinical study titled "Evaluating Procedure Pairing of a Post-Procedure Cream Versus a Comparator in Patients Treated With a Radiofrequency Microneedling for Facial Rejuvenation". This randomized, single-center, double-blinded, controlled, clinical trial was conducted to investigate the tolerability, safety, and efficacy of a post-procedure cream when used immediately after radiofrequency microneedling and for seven days post-procedure with twice daily application in healthy ...
What is the current status of trial NCT06157853?
This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2022-07-11. Estimated completion is 2022-08-23.
What conditions does trial NCT06157853 study?
This clinical trial studies the following conditions: Wrinkle, Photoaging.
What interventions are being tested in trial NCT06157853?
The interventions under investigation include: Radiofrequency Microneedling (PROCEDURE), Facial Cleanser (OTHER), Facial Moisturizer (OTHER), Sunscreen (OTHER).
Who is sponsoring clinical trial NCT06157853?
This trial is sponsored by Revision Skincare, which has 18 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06157853 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Where NCT06157853's enrollment target sits among peer trials
11 24th of 25 higher than 2 of 25 other Wrinkle trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Wrinkle trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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