Outcomes of 20 and 23-gauge Combined Transconjunctival Pars Plana Vitrectomy

This study has been completed.
Sponsor:
Information provided by:
Kocaeli University
ClinicalTrials.gov Identifier:
NCT01176331
First received: August 3, 2010
Last updated: August 5, 2010
Last verified: July 2010
  Purpose

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.


Condition Intervention Phase
Vitrectomy
Procedure: 20 and 23 gauge pars plana vitrectomy
Phase 4

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Outcomes of 20 and 23-gauge Combined Transconjunctival Pars Plana Vitrectomy

Further study details as provided by Kocaeli University:

Primary Outcome Measures:
  • visual acuity

Secondary Outcome Measures:
  • postoperative complications

Groups/Cohorts Assigned Interventions
vitrectomy Procedure: 20 and 23 gauge pars plana vitrectomy

  Eligibility

Ages Eligible for Study:   44 Years to 80 Years
Genders Eligible for Study:   Both
Sampling Method:   Non-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.

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • patients who did not observed periodically during postoperative period.
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01176331

Locations
Turkey
Department of ophthalmology,Hospital of Faculty of Medicine, Kocaeli University
Kocaeli, Turkey
Sponsors and Collaborators
Kocaeli University
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT01176331     History of Changes
Other Study ID Numbers: KOU-8487358664
Study First Received: August 3, 2010
Last Updated: August 5, 2010
Health Authority: Turkey: Ethics Committee

ClinicalTrials.gov processed this record on September 18, 2014