This prospective randomised controlled trial will be conducted to investigate that increasing the vitrectomy cutting rate from 10,000 cut/min to 20,000 cut/min will result more efficiency and shorter core vitrectomy time, and it is equally safe as compared to the current 10,000 cut/min. We plan to target the patients undergoing for vitrectomy for common vitreoretinal pathology. Our plan is to conduct a randomised study with 2 arms, one with the higher cutting rate (20,000 cut/min) versus a second arm using the existing system 10,000 cuts/min.
In addition, we will measure the core vitrectomy duration by Constellation Vision System stopwatch. We will count the duration when the vitrectomy probe enter into the eye to the moment the performing the air/fluid exchange by shaving the peripheral vitreous to complete the vitrectomy. For our second outcome measure to prove the no-inferiority of intraoperative and postoperative complications patients will have 3 months follow up visits.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
72
Vitrectomy blade with increased cutting rate to 20,000 cut/min
Existing Vitrectomy blade with cutting rate 10,000 cut/min
Grantham Hospital
Hong Kong, Hong Kong
Duration of Core vitrectomy
Measurement of core vitrectomy duration by Constellation Vision System
Time frame: intraoperative (From the moment probe enter into the eye till performing the air/fluid exchange to complete the vitrectomy)
Non-inferiority of intraoperative and postoperative complication
Safety and Efficacy
Time frame: 3 months
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