PIONEER: Intraoperative and Perioperative OCT Study

Completed

• Conditions: Retinal Detachment; Epiretinal Membrane; Fuchs Endothelial Dystrophy; Macular Hole

• Registration Number: NCT02423161
• Lead Sponsor: The Cleveland Clinic

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-4-8
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 750

Inclusion Criteria

Inclusion Criteria:<br><br> - The study population includes any patient requiring ophthalmic surgery<br><br>Exclusion Criteria:<br><br> - Children under the age of 18<br><br> - Cognitive/Mentally impaired or unable to provide consent<br><br> - Media opacity precluding OCT scanning

Exclusion Criteria

Not provided

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Feasibility of intraoperative OCT

Secondary Outcome Measures

Name	Time	Method
Utility of intraoperative OCT;Safety of intraoperative OCT;Time requirements for intraoperative OCT