Evaluating Patient Reported Outcomes and Surgeon Satisfaction With Ziplyft™

Recruiting now · Not applicable

Conditions studied: Blepharoplasty

In brief

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.

Key facts

Study ID: NCT07144761
Run by: Osheru Inc.
People needed: 200
Starts: 2025-08-01
Expected to finish: 2025-12-01
Last updated by the study team: 2025-08-27

Who can join

Age: 35 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Provide signed written consent prior to participation in any study-related procedures.
Ability, comprehension, and willingness to follow study instructions, and likely to complete all study visits.
Male or female adults, ≥ 35 years old at the Preoperative Visit
Willing to return for required follow-up visits.
Subjects with excess eyelid skin are eligible to undergo the procedure in the opinion of the investigator.
Female subjects must be 1-year postmenopausal, surgically sterilized, or, if of childbearing potential, have a negative urine pregnancy test at the Preoperative Visit. Women of childbearing potential must use an acceptable form of contraception throughout the study. Acceptable methods include at least one of the following: intrauterine (intrauterine device), hormonal (oral, injection, patch, implant, ring), barrier with spermicide (condom, diaphragm), or abstinence.

You may not qualify if…

Subjects with a current Ptosis diagnosis
Subjects with a history of Graves' Disease
Subjects with Myasthenia Gravis
Subjects that in the opinion of the investigator are anatomically not conducive to using devices (e.g., heavy brow, severe hollowing of the upper eyelid, history of ocular or orbital trauma).
Subjects that have had any previous surgery eyelid or eyebrow region.
Use of anticoagulation therapy, including, but not limited to Aspirin, NSAIDS, Ibuprofen within 7 days and Xarelto, Warfarin, Enoxaparin, Plavix within 3 days prior to planned study procedure.
Active or recent (within 3 months) tobacco user
Allergy to adhesive glue
Participation in any study of an investigational, interventional product within 30 days prior to the Preoperative Visit or at any time during the study period.
Pregnant or nursing females.

Where it is running

Center for Excellence in Eye Care — Miami, Florida, United States (enrolling)
Vance Thompson Vision — Alexandria, Minnesota, United States (enrolling)
Eye Care Specialists — Kingston, Pennsylvania, United States (enrolling)
Vance Thompson Vision — Sioux Falls, South Dakota, United States (enrolling)
The Eye Centers of Racine and Kenosha, LTD — Kenosha, Wisconsin, United States (enrolling)

Full record on ClinicalTrials.gov

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