Clinical Trials Directory

Trials / Completed

CompletedNCT04052633

Success of Intraoperative Cholangiography

Success of Routine Intraoperative Cholangiography

Status
Completed
Phase
Study type
Observational
Enrollment
201 (actual)
Sponsor
Jyväskylä Central Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of the present study was to evaluate the success of routine use of intraoperative cholangiography (IOC ) and to examine the factors that are hindering the performance of intraoperative c-arm cholangiography.

Detailed description

From January 2018 to August 2018 all consecutive elective and emergency cholecystectomies performed were entered in a prospective database. IOC has been instructed to be performed routinely when feasible during cholecystectomy since 1998. All elective operations were performed either by residents or specialist surgeons. For this study the investigators collected the radiation exposure values from exposure and pulsed fluoroscopy. Fluoroscopy time (s) was recorded.The operating surgeon was asked to fulfill a questionnaire directly after the cholecystectomy. The technical success and reasons for possible deferral of IOC were documented.Patient data from unsuccessful or deferred cholangiography cases was checked 6 months after cholecystectomy for possible symptomatic residual choledocholithiasis.Laparoscopic cholecystectomies were performed both by residents and specialist surgeons. Ethics: The study was approved by the hospital administration.

Conditions

Interventions

TypeNameDescription
RADIATIONintraoperative cholangiographysuccess or failure of cholangiography

Timeline

Start date
2018-01-01
Primary completion
2019-03-26
Completion
2019-03-26
First posted
2019-08-12
Last updated
2019-08-12

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT04052633. Inclusion in this directory is not an endorsement.