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Clinical Trial Summary

The primary objective is to describe the safety and efficacy of intravenous sodium fluorescein to visualize ureteral efflux during intraoperative cystoscopy after total laparoscopic hysterectomy. Secondary objective is to report on surgeon's satisfaction with the overall use of sodium fluorescein.


Clinical Trial Description

Thirty patients (n=30) ongoing a total laparoscopic hysterectomy in a tertiary gynecological reference center will be included in this prospective descriptive study.Once hysterectomy is completed, a 10 % solution of sodium fluorescein at a 0,25 ml dose will be injected before performing diagnostic cystoscopy. Time from injection to fluorescent visualization will be recorded as well as coloration density. Adverse events are collected in the operating room, in the recovery room, before patient's discharge and through a home survey. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02971800
Study type Interventional
Source CHU de Quebec-Universite Laval
Contact
Status Completed
Phase N/A
Start date August 2016
Completion date April 2017

See also
  Status Clinical Trial Phase
Completed NCT03432572 - Investigating Oral Agents for Urine Staining to Facilitate Intraoperative Observation of Ureteral Jets Early Phase 1
Withdrawn NCT02757417 - Intravenous Sodium Fluorescein Versus Oral Phenazopyridine for Ureteral Patency N/A
Recruiting NCT04732403 - Ureteral Jets and Patient Positioning Study N/A
Completed NCT04695951 - Efficacy and Safety of Renalof® in the Removal of Calculi Smaller Than 10 mm Located in the Reno-Ureteral Tract Phase 2
Recruiting NCT05477043 - Ureteral Patency After Uterosacral Ligaments Suspension