Endoscopic Cyclophotocoagulation in Normal Tension Glaucoma
Launched by HELSINKI UNIVERSITY CENTRAL HOSPITAL · Nov 26, 2020
Trial Information
Current as of May 06, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new treatment for people with normal tension glaucoma, which is a type of eye condition where the pressure inside the eye is normal, but damage still occurs to the optic nerve. The researchers want to find out if a procedure called endoscopic cyclophotocoagulation, when added to cataract surgery, can help lower eye pressure more effectively than cataract surgery alone. This trial is currently looking for participants who have been diagnosed with normal tension glaucoma and have a significant cataract that needs to be treated.
To be eligible for the study, participants must be adults who can provide consent, have stable glaucoma that is being managed with medication, and show specific signs of nerve damage in their eye. However, people with certain other eye conditions or those who have had previous eye surgeries may not be eligible. If you join the trial, you can expect to receive the standard cataract surgery along with the new treatment to see if it improves your eye pressure better than just the surgery alone. This trial is important as it could lead to better treatment options for those with normal tension glaucoma.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Signed Informed Consent
- • Normal Tension Glaucoma with typical nerve fiber layer defects in red-free photographs and/or optical coherence tomography (OCT) and possible equivalent visual field defects, IOP never more than 21 mmHg, and open anterior chamber angle
- • Glaucoma stable with current medication assessed by a glaucoma specialist
- • Clinically significant cataract
- Exclusion Criteria:
- • Secondary Glaucoma e.g. due to previous injury or uveitis
- • Exfoliation syndrome
- • Pigment dispersion syndrome
- • Previous transscleral or endoscopic cyclophotocoagulation
- • Previous other glaucoma surgery
- • Cataract due to eye injury or congenital cataract
- • Zonular weakness due to Marfan syndrome or other
- • Previous retinal detachment
- • Previous intraocular surgery like vitrectomy and other retinal surgery
- • Wet age-related macular degeneration
- • Diabetic retonopathy
- • Previous corneal transplant or previous refractive surgery
- • Fuchs' dystrophy and other abnormalities compromising corneal clarity like scars
- • The patient does not want to participate in the study
- • The glaucoma progresses on current IOP
- • The patient does not speak Finnish, Swedish or English
- • Dementia
- • Only eye with vision worse than 20/200 or loss of central visual field
About Helsinki University Central Hospital
Helsinki University Central Hospital (HUCH) is a leading academic medical institution in Finland, dedicated to advancing healthcare through innovative research and clinical excellence. As a pivotal sponsor of clinical trials, HUCH integrates cutting-edge medical practices with rigorous scientific inquiry, fostering collaborations between researchers, healthcare professionals, and patients. The hospital is committed to enhancing patient outcomes and contributing to the global body of medical knowledge by conducting high-quality, ethically sound clinical studies across a diverse range of therapeutic areas. With a strong emphasis on education and training, HUCH plays a vital role in shaping the next generation of healthcare leaders and researchers.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Helsinki, , Finland
Patients applied
Trial Officials
Mika Harju, MD, PhD
Principal Investigator
Helsinki University Central Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials