NCT06266962View on ClinicalTrials.gov

Comparing the Efficiency of Two Approaches in Patients at Risk of Developing Intraoperative Floppy Iris Syndrome

PHASE4CompletedINTERVENTIONAL
Enrollment

164

Participants

Timeline

Start Date

July 1, 2020

Primary Completion Date

September 30, 2022

Study Completion Date

September 30, 2022

Conditions
Intraoperative Floppy Iris SyndromeCataractAge-related CataractAdrenergic Receptor Antagonist Adverse Reaction
Interventions
DRUG

1% Atropine drops

Patients administered 1% Atropine drops twice a day for a week before the cataract surgery.

DRUG

Epinephrine

Patients underwent the instillation of epinephrine into the anterior chamber at the beginning of the cataract surgery.

Trial Locations (1)

Unknown

Department of Ophthalmology, University Hospital Olomouc, Olomouc

All Listed Sponsors
collaborator

Palacky University

OTHER

lead

University Hospital Olomouc

OTHER

NCT06266962 - Comparing the Efficiency of Two Approaches in Patients at Risk of Developing Intraoperative Floppy Iris Syndrome | Biotech Hunter | Biotech Hunter