Zeiss RESIGHT Disposable Lenses Evaluation Study

Not Applicable

Completed

• Conditions: Retinal Detachment; Macular Pucker; Macular Holes; Vitreomacular Traction

• Registration Number: NCT05860985
• Lead Sponsor: Universitaire Ziekenhuizen KU Leuven

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-4-13
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion Criteria:<br><br> - Voluntary written informed consent of the participant or their legally authorized<br> representative has been obtained prior to any screening procedures<br><br> - Patients that are scheduled for primary vitrectomy surgery to treat retinal<br> detachment or macular disease (pucker, macular hole, vitreomacular traction).<br><br> - Both vitrectomy-only and combined phaco-vitrectomy surgeries<br><br> - General or local anesthesia, or combination<br><br>Exclusion Criteria:<br><br> - Patient who do not have sufficient command of the Dutch language to read and<br> understand the informed consent form<br><br> - Any disorder, which in the investigator's opinion might jeopardise participant's<br> safety or compliance with the CIP.<br><br> - Repeat vitrectomy surgery

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Ultra Wide Field lens View Angle evaluation;Ultra Wide Field lens Condensation evaluation;Wide Angle lens Condensation evaluation;Illumination appearance evaluation;Color appearance evaluation