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Cholecystectomy Blunt Dissection

Day-care Laparoscopic Cholecystectomy With Diathermy Hook Versus 5mm Suction Irrigation Blunt Dissection: a Randomized Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05366920
Enrollment
20
Registered
2022-05-09
Start date
2022-07-15
Completion date
2023-02-01
Last updated
2022-12-28

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

Conditions

Laparoscopic Cholecystectomy

Keywords

Cholecystolithiasis, Cholelithiasis, Gallstones, Biliary Tract Diseases, Digestive System Diseases, Gallbladder Diseases, Calculi, Pathological Conditions, Anatomical

Brief summary

Day case laparoscopic cholecystectomy can be made with conventional diathermy hook starting at triangle of Calot´s. 5mm suction irrigation blunt dissection starting from the gallbladder fundus is another option. The aim is to test the hypothesis that with 5mm suction irrigation blunt dissection technique a better same day discharge and a shorter operative time can be achieved.

Detailed description

After initiation of general anaesthesia patients are randomized either to conventional(cautery) or 5mm suction irrigation blunt 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

Imam Mohammad ibn Saud Islamic University
Lead SponsorOTHER

Study design

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

Masking description

Single (Participant)

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 frameDescription
number of days for discharge after surgery30 days
operative time30 days
intraoperative bleeding amount30 daysbleeding which require suction or draining

Secondary

MeasureTime frameDescription
type of analgesic and dose30 days
presence of a morbidity30daysnumber of days needed for discharge from service
number of events of postoperative nausea and vomiting which require anti emetic drug30 day
number of days after surgery when readmission is required30 days

Countries

Saudi Arabia

Outcome results

None listed

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