Trials / Recruiting
RecruitingNCT07144761
Evaluating Patient Reported Outcomes and Surgeon Satisfaction With Ziplyft™
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Osheru Inc. · Industry
- Sex
- All
- Age
- 35 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate patient-reported outcomes, surgeon reported outcomes, bruising, symmetry, the success of tissue adhesive for wound closure, and case time.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Ziplyft | Ziplyft™ is a Class 1, 510(k) Exempt device for removing excess unwanted eyelid skin using a novel surgical device called Ziplyft™. |
Timeline
- Start date
- 2025-08-01
- Primary completion
- 2025-12-01
- Completion
- 2025-12-01
- First posted
- 2025-08-27
- Last updated
- 2025-08-27
Locations
5 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07144761. Inclusion in this directory is not an endorsement.