EurEyeCase * Clinical Trial Validation of the EurEyeCase_CT system for robot-assisted retinal surgery
Completed
- Conditions
- Vitreoretinal conditon10047060
- Registration Number
- NL-OMON44615
- Lead Sponsor
- Oogziekenhuis Rotterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 5
Inclusion Criteria
Age * 18 years.
Informed consent.
Vitreoretinal cases with BCVA < 0.5.
Surgery will be performed under general anaesthesia.
Exclusion Criteria
Prognosis of postoperative best corrected visual acuity (BCVA) in the operated eye * 0.3.
Axial length > 28 mm.
Media opacity precluding safe retinal surgery.
BCVA of fellow eye < 0.5.
Use of anticoagulants.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>OCT recordings.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Instrument movement and location.</p><br>