NCT07869108Not yet recruiting
Trabeculectomy Versus MicroShunt Implantation in Glaucoma Surgery (TIGER)
Trabeculectomy Versus MicroShunt Implantation in Glaucoma Surgery: a Randomized Clinical Trial (TIGER)
Source: ClinicalTrials.gov · Last updated 9 Oct 2026
Brief summary (registry, in English)
Glaucoma is an eye disease causing vision loss if not treated adequately. The prevalence is around 1.5%, exponentially increasing to more than 10% in the elderly. Trabeculectomy has been the gold standard surgery for decades and is an evidence based choice for glaucoma surgery. In the last years, new operation methods with shunts or stents (MIGS) have been introduced, however, the scientific evidence for the efficacy and safety of these new methods are scarce and the cost is considerable. Nevertheless, the use has increased, likely due to a shorter learning curve for surgery. The aim of the present project is to perform a randomized clinical trial comparing trabeculectomy versus Preserflo MicroShunt surgery in patients with glaucoma, and to compare the efficacy (intraocular pressure reduction), the safety (in terms of complication rate) and cost-efficiency. The project targets a large patient group and a considerable resource use in Norwegian opthalmology departments. Main aim: to optimize treatment in glaucoma patients by evaluating surgical treatment strategies and guidelines. Objectives: to compare trabeculectomy (gold standard) versus Preserflo microshunt implantation (less invasive surgery) in glaucoma patients in a randomized trial comparing several parameters such as intraocular pressure, number of glaucoma medications, vision and the safety (including complications, corneal endothalial cell loss and need for re-operations) between these two groups.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 27 Sept 2026
- Start date
- 1 Oct 2026
- Primary completion date
- 31 Jan 2028
- Lead sponsor
- Oslo University Hospital
- Diseases
- Glaucoma
- NCT number
- NCT07869108
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 1 Oct 2026 to the primary completion date, 31 Jan 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous filtering surgery in the same eye
Other
- Low target IOP
- Corneal decompensation
- Juvenile glaucoma
Who the study is looking for
- Primary filtering surgery in the given eye
- Ability to cooperate fairly well
- Willingness to participate
Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Department of Ophthalmology, University of Oslo Coordinator of this site? Confirm its status | Oslo | Norway | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.