Oxford, NCNCT07250139Now EnrollingIRB Ready

Dermatochalasis of Upper Eyelid Clinical Trial in Oxford, NC

Access cutting-edge dermatochalasis of upper eyelid treatment through this clinical trial at a research site in Oxford. Study-provided care at no cost to qualified participants.

Sponsored by Osheru Inc.

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Expert Care in Oxford

Access dermatochalasis of upper eyelid specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related dermatochalasis of upper eyelid treatment provided free

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Check if you qualify for this dermatochalasis of upper eyelid clinical trial in Oxford, NC

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Why Participate?

  • No-Cost Study Care

  • Local to Oxford

    Convenient for NC residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Oxford site if eligible
  4. 4Begin participation

About This Dermatochalasis of Upper Eyelid Study in Oxford

This study will compare two surgery techniques used for upper eyelid (eyelift) surgery: traditional surgery and a newer method called Ziplyft (a non-powered, hand-held clamp). This study will use a "split-face" design, meaning one eyelid will be treated with the traditional surgery method and the other with Ziplyft, allowing a direct side-by-side comparison. The objectives of the study are to compare Ziplyft treatment vs. traditional surgery by evaluating bruising, wound closure and incision, surgery case time, and subject/surgeon surveys.

Sponsor: Osheru Inc.

Who Can Participate

Inclusion Criteria

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.

Exclusion Criteria

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.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Oxford?

Yes, this clinical trial (NCT07250139) has an active research site in Oxford, NC that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Dermatochalasis of Upper Eyelid Treatment Options in Oxford, NC

If you're searching for dermatochalasis of upper eyelid treatment options in Oxford, NC, this clinical trial (NCT07250139) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Oxford research site is actively enrolling participants for this clinical trial. You'll receive care from experienced dermatochalasis of upper eyelid specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all dermatochalasis of upper eyelid clinical trials near you to find additional studies recruiting in your area.

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