CompletedNot Applicable

Clinical Outcomes of Implantationof Black Diaphragm Intraocular Lens in Complete Aniridia and Aphakia Due to Posttraumatic Eye Rupture

Poland14 participantsStarted 2006-01-01

Plain-language summary

Purpose: To assess long-term outcomes of implantation of black diaphragmintraocular lens (BD IOL) in postraumatic aniridia and aphakia due to eye rupture. METHODS: This is retrospective consecutive case series of 14 eyes with post-traumatic complete aniridia and aphakia treated withscleral fixation of BD IOL with. Measurements included ophthalmological comorbidities, best corrected visual acuity (BCVA), complications, and postoperative interventions. The average postoperative follow-up period was 36 months.

Who can participate

Age range25 Years – 79 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: post-traumatic complete aniridia and aphakia Exclusion Criteria: active ocluar inflammation or infection

What they're measuring

Best-corrected visual acuity

Timeframe: 10 to 120 months

The slit lamp examination

Timeframe: 10 to 120 months

The intrraocular pressure measurement

Timeframe: 10 to 120 months

The medical history

Timeframe: 10 to 120 months

Trial details

NCT IDNCT03581864

SponsorMedical University of Lublin

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2017-12-31

View on ClinicalTrials.gov More Aphakia Due to Trauma trials