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

History of Changes

Tracking Information
First Received Date ^ICMJE	August 3, 2010
Last Updated Date	August 5, 2010
Start Date ^ICMJE	Not Provided
Primary Completion Date	Not Provided
Current Primary Outcome Measures ^ICMJE (submitted: August 5, 2010)	visual acuity
Original Primary Outcome Measures ^ICMJE	Same as current
Change History	Complete list of historical versions of study NCT01176331 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE (submitted: August 5, 2010)	postoperative complications
Original Secondary Outcome Measures ^ICMJE	Same as current
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Outcomes of 20 and 23-gauge Combined Transconjunctival Pars Plana Vitrectomy
Official Title ^ICMJE	Outcomes of 20 and 23-gauge Combined Transconjunctival Pars Plana Vitrectomy
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.
Detailed Description	Not Provided
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Time Perspective: Retrospective
Target Follow-Up Duration	Not Provided
Biospecimen	Not Provided
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.
Condition ^ICMJE	Vitrectomy
Intervention ^ICMJE	Procedure: 20 and 23 gauge pars plana vitrectomy
Study Group/Cohort (s)	vitrectomy Intervention: Procedure: 20 and 23 gauge pars plana vitrectomy
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Completed
Enrollment ^ICMJE	Not Provided
Completion Date	Not Provided
Primary Completion Date	Not Provided
Eligibility Criteria ^ICMJE	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.
Gender	Both
Ages	44 Years to 80 Years
Accepts Healthy Volunteers	Not Provided
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Turkey

Administrative Information
NCT Number ^ICMJE	NCT01176331
Other Study ID Numbers ^ICMJE	KOU-8487358664
Has Data Monitoring Committee	Not Provided
Responsible Party	Not Provided
Study Sponsor ^ICMJE	Kocaeli University
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	Kocaeli University
Verification Date	July 2010
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

To Top