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NCT01170130

Efficiency and Safety of Lidocaine Usage for Pupil Dilatation (Mydriasis) During Cataract Surgery

Completed NA Last updated 23 February 2015
What this trial tests

NA trial testing Lidocaine 1% (sterile) in Cataract in 100 participants. Completed in 1 October 2012.

Timeline
1 December 2009
Primary endpoint
1 October 2012
1 October 2012

Quick facts

Lead sponsorCarmel Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment100
Start date1 December 2009
Primary completion1 October 2012
Estimated completion1 October 2012

Drugs / interventions tested

Conditions studied

Sponsor

Carmel Medical Center

Who can join

Adults 40 to 80, any sex, with Cataract. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to determine if the mydriatic effect of intracameral lidocaine 1% is as effective as topical cyclopentolate 1% and phenylephrine 10% for achieving effective mydriasis during phacoemulsification surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Cataract

Currently open trials in the same condition.

Other Carmel Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01170130.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing