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Clinical Trials/NCT06364761
NCT06364761
Not yet recruiting
Not Applicable

Assesment of Intermediate and Near Vision After Bag in the Lens Cataract Surgery

Universitair Ziekenhuis Brussel0 sites38 target enrollmentApril 2024
ConditionsCataract

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract
Sponsor
Universitair Ziekenhuis Brussel
Enrollment
38
Primary Endpoint
Intermediate vision
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this observational study is to learn about the intermediate and near vision in patiënts who underwent cataract surgery with a specific technique, called "bag in the lens".

The main question it aims to answer is whether patiens who underwent this type of cataract surgery have better intermediate vision without spectacle correction than patients who underwent the classic lens in the bag cataract surgery.

Participants will:

  • Have to read with and without spectacle correction at different distances (4 meters, 66 centimeters, 40 centimeters)
  • Have to fill in 2 questionnaires about visual functioning and spectacle independance

Researchers will compare these values to the same values from the standard population who underwent the classic lens in the bag cataract surgery with a monofocal intraocular lens .

Registry
clinicaltrials.gov
Start Date
April 2024
End Date
December 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients of at least 18 years old
  • Must have underwent bilateral bag in the lens cataract surgery in the University hospital Brussels at least 3 months before inclusion
  • Must not meet any exclusion criteria

Exclusion Criteria

  • Prior refractive surgery (other than bag in the lens)
  • Corneal opacities
  • Moderate non proliferative diabetic retinopathy or worse
  • Optic neuropathy
  • History of uveitis
  • Amblyopia
  • Residual post-operative astigmatism higher than 1.5 Diopters (D)
  • Best corrected visual acuity \< 1.0
  • Patients unable to cooperate or sign the informed consent

Outcomes

Primary Outcomes

Intermediate vision

Time Frame: During the only hospital visit required in the study, between april and december 2024

uncorrected and distance corrected intermediate vision at 66cm in LogMAR

Secondary Outcomes

  • Near vision(During the only hospital visit required in the study, between april and december 2024)

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