The Royal Alexandra Hospital
Edmonton, Alberta, T5H 3V9, Canada
Location contact
Gurkaran Sarohia, MD
PRINCIPAL_INVESTIGATOR
Mathew Palakkamanil, MD
PRINCIPAL_INVESTIGATOR
Paige Campbell, MD
CONTACT
NCT Number: NCT07285616
Glaucoma refers to a group of progressive optic neuropathies that lead to permanent vision loss. Glaucoma is the leading cause of irreversible blindness globally. In 2020, it was estimated to affect 76 million individuals worldwide, with projections indicating this number will rise to 111.8 million by 2040. In Canada, glaucoma affects an estimated 2.7-7.5% of individuals over the age of 50, contributing substantially to the national disease burden. This condition is linked to damage of the optic nerve due to elevated intraocular pressure (IOP; raised eye pressure), which results in the loss of retinal ganglion cells. Therefore, most of the treatments are guided towards reducing the IOP either via using laser, medications or surgery.
Glaucoma surgery is typically reserved for cases where IOP remains uncontrolled while on maximum tolerated medical therapy and/or where glaucoma progression warrants surgery. The goal of many glaucoma surgeries is to divert aqueous humor from the anterior chamber to the subconjunctival space, therefore reducing intraocular pressure. The device used for this purpose are the PRESERFLO™ MicroShunt (Glaukos Corporation, Laguna Hills, CA, USA) (the documents will interchangeably use terms "stent" and "shunt" to refer to these devices in the text below). The device is implanted using the ab externo approach to channel fluid from the anterior chamber to the subconjunctival/subtenon space. To reduce postoperative fibrosis and inhibit fibroblast activity that could obstruct flow and lead to device failure, 5-fluorouracil (5-FU) or mitomycin C (MMC) are administered. Additionally, a double-layered closure of conjunctiva and Tenon's is performed to minimize Tenon's migration and blockage of tenon the stents. Despite these measures, stent encapsulation and failure are still too common requiring revisions and bleb needling in 2-20% of cases within the first 12 months of follow-up.
This project will involve a series of studies evaluating graft selection in PreserFlo MicroShunt implantation, focusing on donor sclera, cornea, and pericardium as patch graft materials. First, the investigators will conduct a prospective, randomized study comparing clinical outcomes between these graft types. Outcomes of interest will include surgical success rates, post-operative hypotony, tube erosion, conjunctival complications, infection, and overall device longevity. Donor sclera has long been used as a patch graft in glaucoma drainage device surgery and is associated with low erosion rates and reliable long-term results. Corneal tissue is increasingly used due to its transparency and availability through eye banks, with demonstrated safety in ocular surface reconstruction and tube coverage. Pericardium is another durable, biocompatible option, historically applied in both cardiovascular and ocular surgery, and has shown effectiveness as a patch graft in glaucoma drainage implants. This comparison will extend to both primary implantation and revision surgeries, recognizing the high clinical relevance of graft performance in complex cases.
Building on these results, the investigators will then perform a cost-effectiveness analysis of graft strategies, incorporating surgical time, post-operative management, complication rates, and need for re-operation. An economic model will be developed to evaluate costs and resource utilization associated with each material, providing valuable data for policy and surgical decision-making. Finally, the investigators will conduct a patient-reported outcome (PRO) study to assess patient comfort and satisfaction with different grafts. Surveys will evaluate domains such as foreign body sensation, cosmesis, and overall satisfaction at key time points (immediate post-operative period, 1 week, 3 weeks, and 3 months). These results will highlight the patient perspective, an often underrepresented but critical factor in surgical innovation.
Together, these studies will comprehensively assess graft selection from surgical, economic, and patient-centered perspectives, informing evidence-based practice in glaucoma care.
Trial opening soon.
Get Notified18 year–110 year
All sexes
Interventional
Not applicable
Edmonton, Alberta, T5H 3V9, Canada
Gurkaran Sarohia, MD
PRINCIPAL_INVESTIGATOR
Mathew Palakkamanil, MD
PRINCIPAL_INVESTIGATOR
Paige Campbell, MD
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Placement of PreserFlo MicroShunt with donor scleral patch graft to cover the tube.
Placement of PreserFlo MicroShunt with donor corneal patch graft to cover the tube.
Placement of PreserFlo MicroShunt with pericardial patch graft to cover the tube.
Time frame: 12 months
IOP measured by Goldmann applanation tonometry (mmHg) at baseline, post-operative Day 1, Week 1, Month 1, Month 3, Month 6, and Month 12. The primary endpoint will be the mean change at 12 months.
Time frame: 12 months
Proportion of eyes achieving target IOP (≤18 mmHg or ≥20% reduction from baseline) without additional glaucoma surgery, vision-threatening complication, or device removal.
Time frame: 12 months
Number of glaucoma medications used per patient, counted from the medication list at each follow-up (baseline, Month 3, 6, 12). Outcome reported as: Mean change in number of medications.
Time frame: 12 months
Number and percentage of eyes requiring any additional glaucoma or device-related surgery during the study period.
Outcome reported as: Count and proportion of eyes re-operated.
Time frame: 12 months
Number and proportion of eyes requiring bleb needling postoperatively to maintain or restore filtration.
Time frame: 12 months
Clinically confirmed exposure or erosion of tube or patch graft, as documented on slit-lamp exam.
Outcome reported as: Number and percentage of affected eyes.
Time frame: 12 months
IOP < 5 mmHg on two consecutive visits measured by Goldmann applanation tonometry (mmHg).
Outcome reported as: Number and percentage of eyes meeting the definition.
Time frame: 12 months
Any endophthalmitis, blebitis, or wound infection confirmed on clinical exam. Outcome reported as: Number and percentage of eyes with infection.
Time frame: 12 months
BCVA measured using a standard Early Treatment Diabetic Retinopathy Study (ETDRS) chart at 4 m (logMAR scale).
Outcome reported as: Mean change in logMAR from baseline to 12 months (lower values = better vision).
Time frame: Up to 12 months
Time from surgery to defined surgical failure (loss of pressure control, device removal, or re-operation).
Outcome reported as: Kaplan-Meier survival curve; median time to failure.
Time frame: Immediate postop (day 1), 1 week, 3 weeks, 3 months.
Measured using a Visual Analog Scale (VAS, 0-10) where 0 = no discomfort and 10 = worst possible discomfort.
Assessment points: Post-op Day 1, Week 1, Week 3, and Month 3. Outcome reported as: Mean ± SD at each time point.
Time frame: Day 1, 1 week, 3 weeks, 3 months.
Evaluated using a Likert scale (1-5) where 1 = none and 5 = severe sensation. Assessment points: Day 1, Week 1, Week 3, Month 3. Outcome reported as: Mean ± SD and proportion reporting moderate-to-severe sensation (≥4).
Time frame: 3 weeks and 3 months.
Measured with a 5-point Likert scale assessing satisfaction with postoperative appearance (1 = very dissatisfied; 5 = very satisfied).
Assessment points: Week 3 and Month 3. Outcome reported as: Mean ± SD; higher scores = greater satisfaction.
Time frame: 12 months
Number of postoperative visits, additional procedures, and unscheduled urgent encounters recorded per participant from the medical record.
Outcome reported as: Mean count per participant and associated cost estimate (CAD).
Time frame: 12 months
Calculated using trial-based costs and quality-adjusted life-year (QALY) estimates derived from EQ-5D-5L utility weights.
Outcome reported as: Incremental cost per QALY gained by graft type.
Contact information is provided by the study sponsor or research team.
University of Alberta
Other
Optimizing Graft Selection in Glaucoma Surgery
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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