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.