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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | 25 gauge pars plana vitrectomy | 25 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.