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Zeiss RESIGHT Disposable Lenses Evaluation Study

NCT05860985 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2024-08-26

No results posted yet for this study

Summary

To evaluate the intra-operative efficacy of a new intra-operative viewing device.

Conditions

  • Retinal Detachment
  • Macular Pucker
  • Macular Holes
  • Vitreomacular Traction

Interventions

DEVICE

ZEISS disposable

a comparison will be done between the present lenses used (reusable RESIGHT lenses and disposable Vitreq contact lens) and the new disposable RESIGHT lenses.

Sponsors & Collaborators

  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Principal Investigators

  • Peter Stalmans, PhD, MD · UZ Leuven

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-04-11
Primary Completion
2024-07-01
Completion
2024-07-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05860985 on ClinicalTrials.gov