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NCT02836210 · ClinicalTrials.gov registry record · NA

27-gauge Vitrectomy Wound Integrity: a Prospective, Randomized Trial Comparing Angled Versus Straight Entry

A NA study, sponsored by Wills Eye.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT02836210 is a NA study that has completed, run by Wills Eye. The registered enrollment target is 30 participants.

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The verdict

NCT02836210, a NA study, has completed, sponsored by Wills Eye.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

To prospectively compare clinical outcomes using straight (perpendicular) versus angled trocar insertion during 27 gauge pars plana vitrectomy surgery for epiretinal membrane Primary Endpoints: Sclerotomy suture rates and incidence of suture blebs at the end of 27 gauge MIVS. Secondary Endpoints: Rate of postoperative wound-related complications such as hypotony, choroidal detachments, endophthalmitis, and sclerotomy-related retinal tears with a minimum follow-up of 30 days.

Interventions

  • DEVICE 27-gauge vitrectomy wound construction

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2015-05
Est. Completion 2016-10
Phase NA

Sponsor

Wills Eye

59 total trials

What the Registry Record Tells You About NCT02836210

The ClinicalTrials.gov registry entry for NCT02836210 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wills Eye, which has 59 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which 27-gauge vitrectomy wound construction is the first listed.

NCT02836210 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02836210 about?

NCT02836210 is a clinical study titled "27-gauge Vitrectomy Wound Integrity: a Prospective, Randomized Trial Comparing Angled Versus Straight Entry". To prospectively compare clinical outcomes using straight (perpendicular) versus angled trocar insertion during 27 gauge pars plana vitrectomy surgery for epiretinal membrane Primary Endpoints: Sclerotomy suture rates and incidence of suture blebs at the end of 27 gauge MIVS. Secondary Endpoints:...

What is the current status of trial NCT02836210?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2015-05. Estimated completion is 2016-10.

What interventions are being tested in trial NCT02836210?

The interventions under investigation include: 27-gauge vitrectomy wound construction (DEVICE).

Who is sponsoring clinical trial NCT02836210?

This trial is sponsored by Wills Eye, which has 59 total clinical trials registered on ClinicalTrials.gov.

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.