Status:
COMPLETED
Beveled-Tip Versus(vs) Standard-Tip Vitrectomy Probe
Lead Sponsor:
Vanderbilt University Medical Center
Collaborating Sponsors:
Alcon Research
Conditions:
Vitrectomy
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to compare the efficiency of the new Utravit High-Speed 10000 cpm Beveled Probe to the current standard vitrector probe- Alcon (non-beveled) Ultravit 7500 cpm. Study Desi...
Detailed Description
High-speed beveled tip versus standard tip vitrectomy probe: a prospective randomized clinical trial Background: The Advanced Ultravit High-Speed Beveled Probe (Alcon) has a beveled-tip design that ...
Eligibility Criteria
Inclusion
- The study population will be male and female patients 18 years old or older with the presence of pathology requiring routine vitreoretinal surgery (vitreous opacities, vitreous hemorrhage, vitreomacular traction, macular hole, epiretinal membrane) without previous history of vitreoretinal surgery. Ability to consent to procedure.
Exclusion
- Previous incisional intraocular surgery other than uncomplicated cataract surgery with intraocular lens placement
- Inability to consent for procedure
Key Trial Info
Start Date :
September 1 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2022
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT04076072
Start Date
September 1 2019
End Date
January 1 2022
Last Update
October 21 2022
Active Locations (1)
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1
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37232