Preventing angle closure glaucoma in Caucasian patients
Official title: Danish Angle Closure Prevention Trial
Run by University of Aarhus · NCT06077253 · Data updated 2026-11-12
This study tests if a laser treatment can help prevent angle closure glaucoma from getting worse in Caucasian patients who are at risk.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 40 Years to 80 Years |
| Sex | All |
| Enrollment | 242 (estimated) |
| Sponsor | University of Aarhus Academic / other |
| Locations | 5 sites (Aalborg and 4 other locations) |
| Status | Recruiting |
| Started | September 1, 2023 |
| Main results expected | September 1, 2029 |
| Study ends | September 1, 2029 |
| Registry record updated | November 13, 2023 |
| Trial ID | NCT06077253 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are Caucasian individuals identified as primary angle closure suspects with specific clinical criteria.
✕Probably not a fit
Patients with previous eye surgeries, existing glaucoma, or other significant ocular conditions 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
This clinical trial aims to evaluate the effectiveness of prophylactic laser iridotomy in preventing the progression of primary angle closure suspects (PACS) in a Caucasian population. It employs a prospective, randomized paired-eye design, where one eye receives the laser treatment while the other is observed over a five-year follow-up period. The study will assess the outcomes based on the development of angle closure glaucoma and other related complications.
Why it matters
Potential benefit: If successful, this study could provide a preventive treatment option for patients at risk of developing angle closure glaucoma.
How similar studies have gone: Other studies have shown promising results with laser iridotomy in similar populations, indicating potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Primary angle closure suspect: ≥180 degrees (cumulative) irido-trabecular contact on darkroom gonioscopy, IOP\<21mmHg, no peripheral anterior synechiae, no glaucomatous optic neuropathy * Best-corrected visual acuity (BCVA) \>0.8 on both eyes * Caucasian Exclusion Criteria: * Pseudophakia * Previous iridotomy * Clinically significant cataract with indication for surgery, * Gaucoma * Uveitis * Unstable retinal conditions * Ocular malignancies * PEX * PDS * Systemic or ocular corticosteroid treatment
Where it's running
-
Aalborg University Hospital
Aalborg, Denmark Recruiting -
Aarhus University Hospital
Aarhus, Denmark Recruiting -
Rigshospitalet Glostrup
Glostrup Municipality, Denmark Recruiting -
Sygehus Lillebælt
Vejle, Denmark Recruiting -
Odense University Hospital
Odense, Denmark Not yet recruiting
Study contacts
- Principal investigator: Niklas Telinius — Aarhus University Hospital
- Study coordinator: Niklas Telinius, PhD, DMSc
- Email: telinius@me.com
- Phone: +4530238533
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Bioimpedance Spectroscopy for Fluid Changes in Hemodialysis Patients
This study tests whether raw bioimpedance data can help doctors gauge fluid changes in people on hemodialysis and guides fluid removal decisions.
-
PRODIAP: See if patient-reported outcomes improve care for people with type 2 diabetes in general practice
A large Danish trial tests whether using a diabetes-specific patient-reported outcomes questionnaire in general practice helps tailor care for people with type 2 diabetes.
-
Conquer Fear Carer Brief: A Quick Online Therapy for Caregivers Facing Cancer Progression
A short online program helps caregivers of patients with metastatic cancer see if a brief psychological therapy can reduce their fear of cancer progression and be acceptable to them.
-
Tailored rehab for young adults with cancer
This pilot trial tests a youth-focused rehabilitation program called YATAC to see if it’s feasible and acceptable for adults 18-39 with cancer who are in municipal rehab settings.
-
Nitrous Oxide in Blood, Breath, and Urine After Different Exposures
This study tests how nitrous oxide appears in blood, breath, and urine after three different exposures in adults.
-
Disrupted congestion in acute heart failure: can ultrasound at discharge predict readmission and death
This study tests whether ultrasound checks of congestion at discharge can predict which patients with acute heart failure are more likely to be readmitted or die within 90 days.
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.