Reliability of Optical and Ultrasound Biometry in Silicon Filled Eyes

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorSohag University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients with clinical diagnosis of retinal detachment (RD)

planned for pars plana vitrectomy with silicon oil tamponade

Disqualifiers

previous intraocular surgery

failed optical biometry acquisition

recurrent RD

combined scleral buckle surgery

Trial population

number of eyes : 100 eyes data will be collected preoperative and post operative 1 month

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • optical and ulrtasound biometry

    Other intervention

    Optical and ultrasound biometry preoperative and postoperative 1 month

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

axial length

changes in axial length in mm post operative using optical and ultrasound biometry

Time frame
1 month
2

Anterior chamber (AC) depth

changes in AC depth in mm post operative using optical and ultrasound biometry

Time frame
1 month
3

Intra ocular length (IOL) power

changes in IOL power in diopter post operative using optical and ultrasound biometry

Time frame
1 month

Secondary outcomes

Other outcomes

Sponsors and contacts

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