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NCT05689333

A Study to Evaluate the Safety and Performance of the Vista Probe for Vitrectomy Surgery

Completed NA Last updated 1 April 2025
What this trial tests

NA trial testing Vista Vitrectomy Probe in Vitrectomy in 32 participants. Completed in 7 May 2024.

Timeline
9 December 2022
Primary endpoint
7 May 2024
7 May 2024

Quick facts

Lead sponsorVISTA Ophthalmics
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment32
Start date9 December 2022
Primary completion7 May 2024
Estimated completion7 May 2024
Sites4 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

VISTA Ophthalmics

Who can join

18 and older, any sex, with Vitrectomy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, single-arm, non-comparative, open-label, monocular, post approval study to assess safety and device performance of the Vista Vitrectomy Probe during vitrectomy surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05689333.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing