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Day Case Laparoscopic Cholecystectomy: Fundus First With Ultrasonic Dissection or Conventional Diathermy Hook

Day Case Laparoscopic Cholecystectomy: Comparison of Fundus First With Ultrasonic Dissection or Conventional Diathermy Hook, Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01553331
Enrollment
169
Registered
2012-03-14
Start date
2012-03-31
Completion date
2014-10-31
Last updated
2014-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholecystolithiasis

Keywords

laparoscopic cholecystectomy

Brief summary

Day case laparoscopic cholecystectomy can be made with conventional diathermy hook starting at triangle of Calot´s. Ultrasonic dissection starting from the gallbladder fundus is another option. The aim is to test the hypothesis that with ultrasonic dissection technique a better same day discharge and a shorter operative time can be achieved.

Detailed description

After initiation of general anesthesia patients are randomized either to conventional or ultrasonic dissection group. The patients and recovery room personnel are blinded to the operative technique used.

Interventions

Laparoscopic cholecystectomy with diathermy hook starting from triangle of Calot

Sponsors

Central Finland Hospital District
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* ASA I-II * BMI under 35 * normal liver enzymes * no bile duct dilatation in ultrasound * cholecystolithiasis

Exclusion criteria

* NSAID allergy * previous upper gi-surgery * common bile duct stones in preoperative imaging * history of severe acute pancreatitis

Design outcomes

Primary

MeasureTime frame
same day discharge30 days
operative time30 days
intraoperative complications30 days

Secondary

MeasureTime frame
postoperative nausea and vomiting30 days
analgetic use30 days
readmission30 days
morbidity30 days

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026