Clinical Trials Directory

Trials / Completed

CompletedNCT03581864

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

Status
Completed
Phase
Study type
Observational
Enrollment
14 (actual)
Sponsor
Medical University of Lublin · Academic / Other
Sex
All
Age
25 Years – 79 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2006-01-01
Primary completion
2017-12-31
Completion
2018-05-01
First posted
2018-07-10
Last updated
2018-07-10

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT03581864. Inclusion in this directory is not an endorsement.