Tecnis One-Piece Artificial Lens Study R2

Not Applicable

• Conditions: h25; H26; Senile cataract; Other cataract

• Registration Number: DRKS00003633
• Lead Sponsor: AMOVertreter für Europa

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-04-23
• Study Completion: 2012-10-29
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

Healthy patients with bilateral cataract, women shall not be pregnant or breast-feeding

Exclusion Criteria

Uncontrolled systemic or ocular deseases; participation in another trial.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual Acuity after 1 and 3 months postoperatively.

Secondary Outcome Measures

Name	Time	Method
Advers events, patient satisfaction