Efficacy of a New Fixation Method (Intraocular Lens Suspension Method) for Intraocular Lenses (LS-313MF15)

Not Applicable

• Conditions: ens reconstruction patients; Lens sac injury Tearing of the zona pellucida Intraocular lens

• Registration Number: JPRN-jRCT1022230027
• Lead Sponsor: Toru Nakazawa

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-10-17
• Last Update Posted: 20 November 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

(1) Adult patients (18 years of age or older) undergoing lens reconstruction in cases of lens capsule breakage, rupture of the inferior canthus, or fragility of the inferior canthus that may lead to long-term intraocular lens fallout.
(2) Patients who are expected to visit the hospital regularly for at least six months for treatment.
(3) Patients who freely give their consent in writing.

Exclusion Criteria

(1) Cases of corneal opacity to the extent that the fixation status of the intraocular lens cannot be determined.
(2) Patients with retinal or uveal diseases
(3) Patients with a history of allergy to local anesthesia or sedative-analgesic drugs
(4) Patients with a preoperative corneal endothelial cell count of less than 1500 cells
(5) Patients for whom this procedure is found to be technically difficult before or during surgery
(6) Patients whose consent cannot be obtained
(7) Patients who are pregnant or have the possibility of pregnancy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified