Evaluation of postoperative visual function and patient satisfaction with the TECNIS Eyhance Optiblue using the monovision method.

Evaluation of postoperative visual function and patient satisfaction with the TECNIS Eyhance Optiblue using the monovision method. - Evaluation of postoperative visual function and patient satisfaction with the TECNIS Eyhance Optiblue using the monovision method.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000055207

Enrollment

999

Registered

2024-08-25

Start date

2023-08-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cataract

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Patients who used Tecnis Eye Hans OptiBlue or Tecnis Eye Hans OptiBlue Toric II in both eyes 2.Men and women between the ages of 40 and 84 3.Patients with preoperative corneal astigmatism of 2.5 D or less 4.Patients with distance-corrected visual acuity of 1.0 or better at 1 month postoperatively 5.Patients who underwent cataract surgery with binocular correct vision target or mini-monovision method

Exclusion criteria

Exclusion criteria: 1.Patients with a history of LASIK 2.Patients with a history of previous internal ophthalmic surgery 3.Patients with ocular diseases that affect visual function 4.Patients with other systemic or ocular diseases for which the investigator or principal investigator determines that inclusion is inappropriate

Design outcomes

Primary

Measure	Time frame
One month after the second eye surgery, uncorrected distance visual acuity (CDVA and UDVA, respectively), uncorrected intermediate visual acuity at 70 cm (UIVA), and uncorrected near visual acuity at 40 cm (UNVA)	—

Secondary

Measure	Time frame
patient satisfaction	—

Countries

Japan

Contacts

Public ContactYuya Nomura

FUJITA EYE CLINIC Ophthalmology

nomura@fujitaec.or.jp0800-222-1010

Outcome results