Evaluation of the Long-term Efficacy and Safety of Monofocal Plate Haptic Intraocular Lens to be Implanted Into the Eye in Patients Undergoing Cataract Surgery
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
Our study aims to determine the efficacy and safety of the monofocal plate haptic intraocular lens to be implanted in patients planning for cataract surgery and to determine the complications that may develop due to the lens.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Patient informed of the consequences and constraints of the protocol and who has given his/her written informed consent;
• Patients of any gender
• Assured follow-up examinations
• Biometry measurement preferably compatible with the Lenstar evaluation;
• IOL implanted into the capsular bag with IOL model Acriva BB UDM 611 (UVE material) in one or both eyes
Locations
Other Locations
Turkey
Van Yuzuncu Yil University
RECRUITING
Van
Contact Information
Primary
Erbil Seven, MD, Associate Professor
erbilseven@gmail.com
+90 (432) 2150474
Time Frame
Start Date: 2022-11-23
Estimated Completion Date: 2025-05
Participants
Target number of participants: 300
Treatments
Experimental: UDM 611
Acriva BB UDM 611 intraocular lens will be implanted into the capsular bag in patients who undergo cataract extraction with phacoemulsification.
Related Therapeutic Areas
Sponsors
Collaborators: VSY Biotechnology
Leads: Yuzuncu Yıl University