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Efficacy and Safety of the ELIOS Laser in Combined Cataract and Glaucoma Surgery

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Glaucoma is an irreversible optic neuropathy. It is the second most common cause of blindness worldwide. Glaucoma can be treated with topical medications (eye drops), laser or surgery. Traditional surgery is invasive and has a high complication rate (hypotonia, endophthalmitis, cataracts, etc.). As a result, several types of micro-invasive surgery (MIGS) have been developed to reduce the risks of surgery while maintaining their effectiveness in lowering intraocular pressure (IOP). The ELIOS laser system is the only ophthalmological excimer laser designed for the surgical treatment of glaucoma. The aim of the procedure is to ablate the trabecular meshwork and inner wall of Schlemm´s canal ab interno, with the creation of 10 microchannels of 210 um in the trabeculum using the ELIOS laser with a wavelength of 308 nm, in order to improve trabecular outflow to achieve a reduction in IOP. The ELIOS laser is an example of Microinvasive Glaucoma surgery (MIGS) with published results demonstrating efficacy and safety. The ELIOS laser is already in use in France (AMM / CE mark achieved). Its use as part of a prospective interventional study will enable us to collect data in order to treat patients more effectively and improve the quality of care provided to glaucoma patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients ≥ 18 years of age who agree to take part in the study and have signed an informed consent form

• Visually significant cataract with indication for surgery

• Primary open-angle glaucoma, or secondary open-angle glaucoma (pseudoexfoliative glaucoma or pigmentary glaucoma) with indication for cataract surgery.

• Open iridocorneal angle (Shaffer classification grade 2-4)

• Early to moderate glaucoma (advanced glaucoma, with MD from VFs worse than -12dB, will be excluded)

Locations
Other Locations
France
Hôpital Privé de la Baie
RECRUITING
Avranches
Contact Information
Primary
Ana Miguel, MD
myworld_ana@hotmail.com
+33787016187
Time Frame
Start Date: 2025-01-05
Estimated Completion Date: 2028-02-28
Participants
Target number of participants: 46
Treatments
Experimental: Elios
Sponsors
Leads: Hôpital Privé de la Baie

This content was sourced from clinicaltrials.gov