ClinicalTrials.Veeva

Menu

Compare PPV With and Without Silicone Oil in Managing Postoperative Endophthalmitis (Endopthalmitis)

B

Benha University

Status

Completed

Conditions

Endophthalmitis Following Cataract Surgery

Treatments

Procedure: Silicone Oil
Procedure: Pars plana Vitrectomy

Study type

Interventional

Funder types

Other

Identifiers

NCT06990607
Endophthalmitis and silicone

Details and patient eligibility

About

Comparing PPV with and without silicone oil in managing postoperative endophthalmitis

Full description

The objective of this study is to compare the outcomes of PPV with silicone oil tamponade to PPV alone in patients with postoperative endophthalmitis by assessing visual acuity, and postoperative complications such as rhegmatogenous retinal detachment (RRD).

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adult patients (≥ 18 years) presenting with clinical manifestations of endophthalmitis after cataract surgery

Exclusion criteria

  • patients with concurrent ocular or systemic conditions that could potentially confound study outcomes, such as active retinal diseases unrelated to endophthalmitis
  • pre-existing poor visual prognosis due to conditions like advanced glaucoma or macular degeneration, or prior ocular surgery affecting the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Group I
Active Comparator group
Description:
Pars plana Vitrectomy Alone
Treatment:
Procedure: Pars plana Vitrectomy
Group II
Active Comparator group
Description:
Pars plana Vitrectomy with Silicone Oil
Treatment:
Procedure: Pars plana Vitrectomy
Procedure: Silicone Oil

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems