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

NCT03581864 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 14

Last updated 2018-07-10

No results posted yet for this study

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

  • Aphakia Due to Trauma
  • Eye; Rupture, Traumatic, With Loss of Intraocular Tissue
  • Aniridia

Sponsors & Collaborators

  • Medical University of Lublin

    lead OTHER

Eligibility

Min Age
25 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-01
Primary Completion
2017-12-31
Completion
2018-05-01

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03581864 on ClinicalTrials.gov