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NCT04076072 · ClinicalTrials.gov registry record · NA
Beveled-Tip Versus(vs) Standard-Tip Vitrectomy Probe
A NA study of Vitrectomy, sponsored by Vanderbilt University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 1
- Study location
NCT04076072 is a NA study of Vitrectomy that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 40 participants. The trial reports 1 study location across 1 state.
The verdict
NCT04076072, a NA study of Vitrectomy, has completed, sponsored by Vanderbilt University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 1
- Study location
Study 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 Design: This is a randomized controlled trial comparing the efficiency of the Ultravit High-Speed Beveled Probe with the current Alcon vitrector probe in a cohort of patients undergoing routine vitrectomy surgery. Hypothesis: The Advanced Ultravit high-speed beveled probe will show non-inferiority to the standard, Alcon (non-beveled) Ultravit 7500 cpm with regards to time to completion of vitrectomy and surgical outcomes.
Conditions Studied
Interventions
- DEVICE Utravit High-Speed 10000 cpm Beveled Probe
- DEVICE standard vitrector probe- Alcon (non-beveled) Ultravit 7500 cpm
Study Locations (1)
Tennessee
- Vanderbilt University Medical Center - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2019-09-01 |
| Est. Completion | 2022-01-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04076072
The ClinicalTrials.gov registry entry for NCT04076072 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Vitrectomy appearing as the primary indexed condition, and to 2 interventions - of which Utravit High-Speed 10000 cpm Beveled Probe is the first listed.
NCT04076072 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT04076072 about?
NCT04076072 is a clinical study titled "Beveled-Tip Versus(vs) Standard-Tip Vitrectomy Probe". 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 Design: This is a randomized controlled trial comparing the efficiency of the Ultravit High-Speed Bevel...
What is the current status of trial NCT04076072?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2019-09-01. Estimated completion is 2022-01-01.
What conditions does trial NCT04076072 study?
This clinical trial studies the following conditions: Vitrectomy.
What interventions are being tested in trial NCT04076072?
The interventions under investigation include: Utravit High-Speed 10000 cpm Beveled Probe (DEVICE), standard vitrector probe- Alcon (non-beveled) Ultravit 7500 cpm (DEVICE).
Who is sponsoring clinical trial NCT04076072?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04076072 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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