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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03581864

Enrollment

Registered

2018-07-10

Start date

2006-01-01

Completion date

2018-05-01

Last updated

2018-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

aphakia, black diaphragmintraocular lens, eye rupture, aniridia

Brief 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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

25 Years to 79 Years

Healthy volunteers

Inclusion criteria

post-traumatic complete aniridia and aphakia

Exclusion criteria

active ocluar inflammation or infection

Design outcomes

Primary

Measure	Time frame	Description
Best-corrected visual acuity	10 to 120 months	The visual acuity measurement with ETDRS chart
The slit lamp examination	10 to 120 months	The anterior segment of the eye and eye fundus were examined.
The intrraocular pressure measurement	10 to 120 months	The procedure was performed with the Goldman applanation tonometer.
The medical history	10 to 120 months	Coexisting eye diseases and post-operative complications were noted.

Countries

Poland

Outcome results