Comparison of Efficacy Between ILM Forceps
Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age19+
SponsorUniversity of British Columbia
About this trial
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).
Eligibility criteria
Qualifiers
None
Disqualifiers
Co-morbid diabetic retinopathy of any grade.
Neovascular AMD.
Previous vitrectomy.
Previous retinal detachment treated with scleral buckle or pneumatic retinopexy.
Trial design
Treatments tested in this trial
- Internal limiting membrane (ILM) Peeling with Sharkskin Forceps
- Internal limiting membrane (ILM) Peeling with Standard Forceps
Treatment groups
56 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of British Columbia
Lead sponsor
Sengi
Collaborator
Source ClinicalTrials.gov