EurEyeCase * Clinical Trial Validation of the EurEyeCase_CT system for robot-assisted retinal surgery

EurEyeCase * Clinical Trial Validation of the EurEyeCase_CT system for robot-assisted retinal surgery - EurEyeCase_CT

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON44615

Enrollment

Registered

2017-11-16

Start date

2018-02-13

Completion date

Unknown

Last updated

2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vitreoretinal conditon

Interventions

Insertion of the OCT probe in the eye and intraocular manipulation.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age * 18 years. Informed consent. Vitreoretinal cases with BCVA

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
OCT recordings.	—

Secondary

Measure	Time frame
Instrument movement and location.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)