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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01176331
Enrollment
Unknown
Registered
2010-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2010-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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.

Interventions

PROCEDURE20 and 23 gauge pars plana vitrectomy

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
44 Years to 80 Years

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.

Design outcomes

Primary

MeasureTime frame
visual acuity—

Secondary

MeasureTime frame
postoperative complications—

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026