Registry study for quality control and optimization of postoperative outcomes of ocular implants.

Recruiting

• Conditions: H25.1; T85.2; H26.4; Senile nuclear cataract; Mechanical complication of intraocular lens; After-cataract

• Registration Number: DRKS00007837
• Lead Sponsor: International Vision Correction Research Centre (IVCRC), UNiversitäts-Augenklinik Heidelberg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-03-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 2000

Inclusion Criteria

Condition following monocular or binocular fitting with an ophthalmic implant, female and male > 18 years, written informed consent, legal capacity

Exclusion Criteria

Dementia, pregnancy and lactation

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Deviation target vs. achieved postoperative refraction (for IOL constant optimization) after 3 month only

Secondary Outcome Measures

Name	Time	Method
Functional results (refraction, visual acuity), subjective Patient satisfaction, Quality of Vision (contrast, spherical Aberration), stability of postoperative achieved results<br>Preoperative data is evaluated retrospectively from pseudonymisiced patient files. The patients will be rescheduled for all examinations after 3 month, 1 year and 3 years.<br>Patient satisfaction will be evaluated by self developed subjective questionaire