Clinical Trials Directory

Trials / Completed

CompletedNCT04902170

Long-shaft Vitrectomy Probe in Highly Myopic Eyes

The Surgical Outcomes of Long-shaft Vitrectomy Probe for Vitreoretinal Diseases in Highly Myopic Eyes

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
86 (actual)
Sponsor
National Taiwan University Hospital · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

This study aimed to compare the safety and efficacy of vitrectomy probe with different shaft lengths in vitreoretinal surgery of highly myopic patients. In this randomized controlled study, highly myopic patients who had axial length more than 26 mm and needed vitreoretinal surgery will be enrolled. The enrolled patients will be randomized into "30 mm shaft length group"(trial group) and "27mm shaft length group"(controlled group). We will compare the rate of wound leakage, hypotony, subconjunctival hemorrhage, probe bending, trocar removal, and endophthalmitis between the two groups. We would like to evaluate the efficacy and safety of the 30 mm shaft length vitrectomy probe.

Conditions

Interventions

TypeNameDescription
PROCEDURE25 gauge pars plana vitrectomy25 gauge pars plana vitrectomy

Timeline

Start date
2021-07-22
Primary completion
2022-06-17
Completion
2023-02-07
First posted
2021-05-26
Last updated
2023-06-18

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04902170. Inclusion in this directory is not an endorsement.