Rotational Stability and Clinical Response of the ASQELIO Toric Biaspheric Monofocal Lens.

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

The goal of this observational study is to evaluate the rotational stability and clinical performance of the ASQELIO Toric lens in candidates for cataract surgery with ASQUELIO Toric intraocular lens (IOL) implantation. Information will be obtained from patients operated by routine clinical practice with toric monofocal ASQELIO IOL in at least one eye. After confirmation of inclusion, the preoperative examination will be performed, and after surgery an evaluation will be performed the following day, one week, one month and three months after surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:

• Subjects 22 years of age or older undergoing cataract surgery in at least 1 eye and implanted with LIO ASQELIO.

• Subjects for whom postoperative emmetropia was planned (±0.5 D spherical equivalent)

Locations
Other Locations
Spain
Oftalvist Alicante
RECRUITING
Alicante
OftalVist Madrid
RECRUITING
Madrid
OftalVist Valencia
RECRUITING
Valencia
Contact Information
Primary
Maria Cobo, Dr
maria.cobo@oftalvist.es
+34963513304
Time Frame
Start Date: 2024-02
Estimated Completion Date: 2024-10
Participants
Target number of participants: 63
Treatments
Pseudophakic subjects implanted with the ASQELIO toric IOL
Adult subjects undergoing cataract surgery by routine clinical practice with ASQELIO Toric Biaspheric Monofocal Lens in at least one eye.
Related Therapeutic Areas
Sponsors
Leads: AST Products, Inc.

This content was sourced from clinicaltrials.gov