Diabetic Retinopathy Clinical Trial
Official title:
A Prospective, Randomised Controlled Trial of Ranibizumab Pre-treatment in Diabetic Vitrectomy - a Pilot Study
This study will evaluate the effect of ranibizumab on patients undergoing vitrectomy surgery
for the complications of diabetic retinopathy.
Vitrectomy surgery can be difficult and bleeding after the operation can reduce vision for
patients. Our hypothesis is that injection into the eye of ranibizumab one week before
surgery will make the surgery easier, reduce complications and improve outcome.
In this trial, patients will be randomly allocated to receive either ranibizumab injection or
a placebo injection of saline. Neither the patient, their surgeon, nor the study
investigators will know which they have received so that a fair comparison can be made.
The RaDiVit study is a pilot randomised controlled trial to evaluate the effect of
ranibizumab as an adjunct to diabetic vitrectomy surgery.
Patients with complications of proliferative diabetic retinopathy who require vitrectomy
surgery will be recruited to this study. Baseline tests will be performed, including
refracted visual acuity, B-scan ultrasound, OCT scanning, colour fundus photography and
fundus fluorescein angiography. Patients will be randomised 1:1 to receive either ranibizumab
intravitreal injection or saline subconjunctival injection.
One week later, surgery will be carried out. The baseline tests will be repeated on the day
of surgery to examine for any discernible difference between the two groups one week after
treatment. Surgery will be video recorded and detailed assessments of the operative details
carried out.
A vitreous sample and a paired serum sample will be taken at the time of surgery to compare
levels of ranibizumab and related cytokines.
Follow up visits will take place at six and twelve weeks. Assessments at that point will
include:
- visual acuity
- OCT scan
- colour fundus photography and fundus fluorescein angiography
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