Evaluation of Patient and Physician Satisfaction With the Zift eLevatIon of Facial Tissue Clinica… (NCT03055819) | Clinical Trial Compass
TerminatedNot Applicable
Evaluation of Patient and Physician Satisfaction With the Zift eLevatIon of Facial Tissue Clinical Study
Stopped: Company no longer exists
United States20 participantsStarted 2017-02-03
Plain-language summary
The LIFT study will document the first clinical use of the ZiftLift Tissue Anchor in a browlift for patients with age-related brow ptosis. It is a single arm, open label multicenter study, to evaluate the safety and efficacy of the Zift Lift System. Up to 20 subjects in up to 3 sites will be enrolled in this study. Data from this trial will be used to confirm the device safety and efficacy and provide inputs to further refine the device design and procedure technique for future device iterations
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion criteria
✓. Able to provide informed consent to the treatment
✓. Willing and able to participate in all the required follow-ups
✓. Over 18 years of age
✓. Under 75 years of age
✓. Brow ptosis and/or functional limitations such as vision defects due to tissue laxity caused by aging
Exclusion criteria
✕. Known allergies to local anesthesia
✕. Currently undergoing chemotherapy or radiation therapy for cancer
✕. Known advanced osteoporosis that may lead to skull thinning
✕. Taking long-term immunosuppressant therapy
✕. Taking chronic anticoagulation therapy (including ASA and NSAIDS) which can't be stopped for 10 days before treatment.