Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID02423213

Determination of Feasibility of Intraoperative Spectral Domain Microscope Combined/Integrated OCT Visualization During En Face Retinal and Ophthalmic Surgery: DISCOVER Study

Led by The Cleveland Clinic · Updated on 2025-06-26

3000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

T

The Cleveland Clinic

Lead Sponsor

N

National Eye Institute (NEI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research focuses on using optical coherence tomography (OCT), a technology that provides detailed, high-resolution images of the eye's tissue in both cross-sectional and three-dimensional views. It explores the potential benefits of integrating OCT directly into the surgical microscope during eye surgeries, allowing surgeons to better understand how their procedures affect the eye's anatomic structure. This observational study aims to assess the feasibility and usefulness of this integrated OCT system during ophthalmic surgeries for various retinal and eye conditions. The study uses an OCT device built into the surgical microscope rather than a separate or hand-held system. This integration may offer advantages such as improved efficiency, better working distance, and the ability to see how surgical instruments interact with eye tissue in real time. Images will be taken at different stages during surgery to evaluate the functionality and potential impact of this technology. Participants will be patients undergoing ophthalmic surgery, and the study involves capturing intraoperative OCT images during these procedures. Researchers will assess how feasible it is to use this integrated OCT system and how it might influence surgical decisions. The study will monitor outcomes related to the use of this technology over a three-year period. Participants' usual care continues as normal, and the overall participation spans the time of their surgical procedure and associated evaluations.

CONDITIONS

Brief Title

DISCOVER Study: Microscope-integrated Intraoperative OCT Study

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients requiring ophthalmic surgery
  • Age 18 years or older
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Under the age of 18 years
  • Cognitive or mental impairment preventing informed consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Day of surgery

Participants undergo ophthalmic surgery during which microscope-integrated intraoperative OCT imaging is used at various milestones to assess feasibility and utility.

1 surgical visit (in-person)

Post-operative Follow-up

Duration - Up to 3 years

Participants are observed after surgery to monitor outcomes and assess the impact of intraoperative OCT on surgical decision-making.

Visits scheduled as part of routine post-operative care

Trial Site Locations

Total: 1 location

1

Cole Eye Institute, Cleveland Clinic

Cleveland, Ohio, United States, 44195

Actively Recruiting

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Research Team

J

Justis P Ehlers, M.D.

J

Jamie L Reese, R.N.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Integrative advances for OCT-guided ophthalmic surgery and intraoperative OCT: microscope integration, surgical instrumentation, and heads-up display surgeon feedback.

Justis P Ehlers, Sunil K Srivastava, Daniel Feiler...

https://pubmed.ncbi.nlm.nih.gov/25141340

Intraoperative optical coherence tomography using the RESCAN 700: preliminary results from the DISCOVER study.

Justis P Ehlers, Peter K Kaiser, Sunil K Srivastava

https://pubmed.ncbi.nlm.nih.gov/24782469