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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: Completed NA study, sponsored by Wills Eye.

NCT02836210 is a NA study that has completed, run by Wills Eye. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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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
Wills Eye

59 total trials

What the finished NCT02836210 record still lists

NCT02836210 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT02836210 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT02836210's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02836210, the US trial registry maintained by the National Library of Medicine. NCT02836210 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.