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Comparison of Efficacy Between ILM Forceps

NCT06536569 · Status: NOT_YET_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2025-03-30

No results posted yet for this study

Summary

This study is a Single center, prospective, observational, multi surgeon randomized controlled trial. Subjects will be assessed pre-operatively, operatively and at 1 month postoperatively. Clinical evaluations will include measurement of visual acuity and optical coherence tomography (OCT).

Conditions

  • Macular Holes
  • Epiretinal Membrane

Interventions

DEVICE

Internal limiting membrane (ILM) Peeling with Sharkskin Forceps

25g Grieshaber Sharkskin ILM Forceps with Reflex Handle

DEVICE

Internal limiting membrane (ILM) Peeling with Standard Forceps

25g Grieshaber Standard ILM Forceps

Sponsors & Collaborators

  • Sengi

    collaborator INDUSTRY

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Bryon McKay, MD, PhD · UBC

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-01
Primary Completion
2025-12-01
Completion
2026-01-01
FDA Device
Yes

Countries

  • Canada

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 NCT06536569 on ClinicalTrials.gov