Micro-invasive surgery for glaucoma treatment
Official title: NorMIGS - a Prospective Study of Micro-invasive Glaucoma Surgery
Run by Oslo University Hospital · NCT05340647 · Data updated 2026-11-12
This study is testing a new micro-surgery for glaucoma to see if it works better and has fewer problems than traditional surgeries for patients needing treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Oslo University Hospital Academic / other |
| Locations | 1 site (Oslo) |
| Status | Recruiting |
| Started | April 22, 2022 |
| Main results expected | December 2023 |
| Study ends | June 2028 |
| Registry record updated | November 29, 2022 |
| Trial ID | NCT05340647 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who are scheduled for implantation of the Preserflo microshunt, trabeculectomy, or other micro-invasive glaucoma surgeries.
✕Probably not a fit
Patients with high intraocular pressure due to conditions like hemorrhagic glaucoma, traumatic glaucoma, or uveitis glaucoma may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
NorMIGS is an observational study that evaluates the effectiveness and complications of the Preserflo microshunt implantation compared to other glaucoma surgeries, such as trabeculectomy. Conducted at the Department of Ophthalmology at Oslo University Hospital, the study aims to gather data on intraocular pressure reduction and patient outcomes. Participants will be monitored for their ability to cooperate during examinations and provide informed consent. The study includes patients scheduled for various types of glaucoma surgery.
Why it matters
Potential benefit: If successful, this study could provide insights into safer and more effective surgical options for glaucoma patients.
How similar studies have gone: Other studies have shown promising results with micro-invasive glaucoma surgeries, indicating that this approach is gaining traction in the field.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients must be 18 years or older at the time of signing the informed consent form. There is no upper age limit. * Scheduled for implantation of Preserflo microshunt, trabeculectomy or other types of MIGS * Ability to cooperate fairly well during the examinations * Willing to participate in the study and capable of providing informed consent Exclusion Criteria: \- High intraocular pressure due to increased episcleral venous pressure, hemorrhagic glaucoma, traumatic glaucoma or uveitis glaucoma
Where it's running
-
Department of Ophthalmology, Oslo University Hospital
Oslo, Norway Recruiting
Study contacts
- Principal investigator: Olav Kristianslund, MD PhD — Department of Ophthalmology, Oslo University Hospital
- Study coordinator: Olav Kristianslund, MD PhD
- Email: olakri@ous-hf.no
- Phone: +4722118545
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Long-Term Results After Ab-interno Trabeculotomy for Glaucoma
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.