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Recruiting NCT07731984

Reliability of Optical and Ultrasound Biometry in Silicon Filled Eyes

— Observational Retinal Detachment

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: optical and ulrtasound biometry.
Who it may be relevant to
Registry conditions: Retinal Detachment. Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Optical and ultrasound biometry will be done for Patients who will undergo pars plana vitrectomy (PPV) and silicon oil injection preoperative and post operative 1 month

Detailed description

Optical and ultrasound biometry will be done for Patients who will undergo PPV and silicon oil injection preoperative and post operative 1 month , patients will be subdevided into 2 groups PPV with silicon oil tamponade and another group phacovitrectomy with silicon oil tamponade for assesment of postoperative refraction

Interventions

  • Other optical and ulrtasound biometry
    Optical and ultrasound biometry preoperative and postoperative 1 month

Primary outcome measures

  • axial length [Time frame: 1 month]
  • Anterior chamber (AC) depth [Time frame: 1 month]
  • Intra ocular length (IOL) power [Time frame: 1 month]

Eligibility criteria

Inclusion criteria

  • patients with clinical diagnosis of retinal detachment (RD)
  • planned for pars plana vitrectomy with silicon oil tamponade

Exclusion criteria

  • previous intraocular surgery
  • failed optical biometry acquisition
  • recurrent RD
  • combined scleral buckle surgery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Egypt · 1 center
  • Faculty of Medicine Sohag University — Sohag

Identifiers

NCT: NCT07731984 · Soh-Med-26-3-1MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗