Tecnis One-Piece Artificial Lens Study R2

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00003633

Enrollment

Registered

2012-04-23

Start date

2012-02-21

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

h25 H26

Interventions

Group 1: One eye receives the study lens, the other eye the control lens. A randomization is done to determine, which lens will be implanted into the first eye. Group 2: bilateral implantation of stud

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: Uncontrolled systemic or ocular deseases; participation in another trial.

Design outcomes

Primary

Measure	Time frame
Visual Acuity after 1 and 3 months postoperatively.	—

Secondary

Measure	Time frame
Advers events, patient satisfaction	—

Countries

Austria, Germany

Contacts

Public ContactRoland Pohl

AMO Vertreter für Europa

roland.pohl@amo.abbott07243-729451

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026