NCT01176331

Brief Summary

In a retrospective study, a combined 20 and 23-gauge pars plana vitrectomy procedure was performed in 21 eyes for various indications and proposed as a transition procedure to 23-gauge transconjunctival vitrectomy. Through use of combination of procedures postoperative complications, surgical trauma and healing time was decreased; operating time was reduced; costs were decreased.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 3, 2010

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 6, 2010

Completed
Last Updated

August 6, 2010

Status Verified

July 1, 2010

First QC Date

August 3, 2010

Last Update Submit

August 5, 2010

Conditions

Vitrectomy

Outcome Measures

Primary Outcomes (1)

  • visual acuity

Secondary Outcomes (1)

  • postoperative complications

Study Arms (1)

vitrectomy

Procedure: 20 and 23 gauge pars plana vitrectomy

Interventions

20 and 23 gauge pars plana vitrectomyPROCEDURE
vitrectomy

Eligibility Criteria

Age44 Years - 80 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who were in the range 44 to 80 years, who had to undergo vitrectomy operation with different diagnosis were included in the study. Each participant had a complete ophthalmological examination which included best-corrected visual acuity (BCVA), slit lamp examination with and without pupil dilation, intraocular pressure (IOP) measurement with applanation tonometry and stereoscopic evaluation of the ocular fundus before decision of operation.

You may qualify if:

  • eyes requiring pars plana vitrectomy for various indications: such as dropped lens, intraocular blood, retinal detachments...etc.

You may not qualify if:

  • patients who did not observed periodically during postoperative period.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of ophthalmology,Hospital of Faculty of Medicine, Kocaeli University

Kocaeli, Turkey (Türkiye)

Location

Study Design

Study Type
observational
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 3, 2010

First Posted

August 6, 2010

Last Updated

August 6, 2010

Record last verified: 2010-07

Locations

TU(1)