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NCT03228641 · ClinicalTrials.gov registry record · NA
Evaluation of Safety and Efficacy of Micro-coring Device for Treatment of Facial Wrinkles and Skin Laxity
A NA study of Wrinkle and Facial and Neck Skin Laxity, sponsored by Cytrellis Biosystems.
- Completed
- Registry status
- NA
- Development phase
- 33
- Enrollment target
- 5
- Study locations
NCT03228641 is a NA study of Wrinkle and Facial and Neck Skin Laxity that has completed, run by Cytrellis Biosystems. The registered enrollment target is 33 participants, below the 119-participant average among 25 other Wrinkle trials with a reported enrollment target (72% lower). The trial reports 5 study locations across 5 states.
The verdict
NCT03228641, a NA study of Wrinkle and Facial and Neck Skin Laxity, has completed, sponsored by Cytrellis Biosystems.
- COMPLETED
- Registry status
- NA
- Development phase
- 33 participants
- Enrollment target
- 5
- Study locations
Study Summary
A pilot study is designed to evaluate safety and efficacy of the Micro-Coring (MC) technology for treatment of facial wrinkles. MC device employs hollow coring needles that enable safe, rapid, and effective full-thickness small skin cores (200-500 microns in diameter) removal initiating a skin repair process through formation of new collagen and elastin fibers (skin rejuvenation).
Conditions Studied
Interventions
- DEVICE micro-excisional skin removal with coring needle
Study Locations (5)
California
- Laser & Skin Center of Northern CA - Sacramento
Massachusetts
- SkinCare Physicians - Chestnut Hill
New York
- Laser & Skin Surgery Center of NY - New York
Tennessee
- Nashville Center for Laser & Facial Surgery - Nashville
Texas
- Dr A Jay Burns Cosmetic Surgery - Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2016-06-01 |
| Est. Completion | 2018-04-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03228641
The ClinicalTrials.gov registry entry for NCT03228641 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 119-participant average among 25 other Wrinkle trials with a reported enrollment target (72% lower). The listed sponsor is Cytrellis Biosystems, which has 8 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Wrinkle appearing as the primary indexed condition, and to 1 intervention - of which micro-excisional skin removal with coring needle is the first listed.
NCT03228641 reports 5 study locations spanning 5 distinct geographic areas - top geographies include California, Massachusetts, New York.
Frequently Asked Questions
What is clinical trial NCT03228641 about?
NCT03228641 is a clinical study titled "Evaluation of Safety and Efficacy of Micro-coring Device for Treatment of Facial Wrinkles and Skin Laxity". A pilot study is designed to evaluate safety and efficacy of the Micro-Coring (MC) technology for treatment of facial wrinkles. MC device employs hollow coring needles that enable safe, rapid, and effective full-thickness small skin cores (200-500 microns in diameter) removal initiating a skin repai...
What is the current status of trial NCT03228641?
This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2016-06-01. Estimated completion is 2018-04-30.
What conditions does trial NCT03228641 study?
This clinical trial studies the following conditions: Wrinkle, Facial and Neck Skin Laxity.
What interventions are being tested in trial NCT03228641?
The interventions under investigation include: micro-excisional skin removal with coring needle (DEVICE).
Who is sponsoring clinical trial NCT03228641?
This trial is sponsored by Cytrellis Biosystems, which has 8 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03228641 being conducted?
This trial has 5 study locations across California, Massachusetts, New York, Tennessee, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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