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INTRAOCULAR PRESSURE MEASUREMENT AT the END of PARS PLANA VITRECTOMY

Not Applicable
Not yet recruiting
Conditions
Pars Plana Vitrectomy
Registration Number
NCT06707168
Lead Sponsor
Sunnybrook Health Sciences Centre
Brief Summary

Intraocular pressure is measured regularly at any and all visits with your eye doctor or optometrist.

The purpose of this study is to compare measurements of eye pressure at the end of the surgery, comparing the ability of a gloved finger or sterile cotton-tipped applicator ("Q-tip") to accurately measure intraocular pressure against a standardized instrument designed for this purpose.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  1. All patients undergoing Pars Plana Vitrectomy between June 25, 2024 - and December 30, 2024, will be included.
  2. Patients aged 18 years or older
  3. Patients able to give informed consent
Exclusion Criteria
  1. Patients with complicated Pars Plana Vitrectomy (choroidal hemorrhage, retrobulbar hemorrhage)
  2. Patients with irregular cornea surface will be excluded (keratoconus, band keratopathy, corneal edema, corneal transplant, cornea scarring)
  3. Patients undergoing combined scleral buckling at time of surgery
  4. Patients with previous glaucoma filtration surgery (ie. trabeculectomy or tube shunt surgery)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Intraocular pressure measurementFrom enrolment to end of treatment at 8 weeks

Intraocular pressure accuracy between surgeons' estimate and tonometer IOP measurement.

Secondary Outcome Measures
NameTimeMethod
Intraocular pressure measuring agreementFrom enrolment to end of treatment at 8 weeks

1. Intraocular pressure surgeon measuring agreement with digital palpation.

2. Intraocular pressure surgeon measuring agreement with short wooden stick cotton swab.

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