Clinical trial

Safety and Efficacy Trial to Evaluate the Hydrus(TM) Implant in Subjects Undergoing Cataract Surgery.

NCT01818115

Drugs and interventions used in this trial

2 registered

These interventions are listed by ClinicalTrials.gov. An RxNorm link indicates a mapped medicine record; the registry name alone is not proof of a specific branded formulation.

Search this trial's interventions

DEVICE · Unmapped registry intervention Hydrus Implant Find medicine records · Find other trials using this name

PROCEDURE · Unmapped registry intervention IOL placement Find medicine records · Find other trials using this name

Study at a glance

Registry-backed

Safety and Efficacy Trial to Evaluate the Hydrus(TM) Implant in Subjects Undergoing Cataract Surgery.

Design: INTERVENTIONAL · Status: COMPLETED · Phase: NA

Read study objectives, eligibility and outcome measures at ClinicalTrials.gov

StatusCOMPLETED

Study typeINTERVENTIONAL

Start date2011-01-01

PhaseNA

Conditions

Primary Open Angle Glaucomaunresolved

Glaucoma, Open Angle, Pseudo-exfoliativeunresolved

Cataract Unilateral Pending Extractionunresolved

Interventions

Hydrus ImplantDEVICE

IOL placementPROCEDURE

Sponsors & collaborators

Ivantis, Inc.lead sponsor

Mapped research locations

MadridSpain1 FrankfurtGermany1 RotterdamNetherlands1 MainzGermany1 ZaragozaSpain1 TorinoItaly1

Registry source

Open the source record to verify current eligibility, contacts, locations and registry updates.

Open NCT01818115 on ClinicalTrials.gov ↗

Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.