Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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.

View on ClinicalTrials.gov ↗

View your shortlist →

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

FieldValue
Enrollment Target 40 participants
Start Date 2019-09-01
Est. Completion 2022-01-01
Phase NA

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.

Similar trials for Vitrectomy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.