- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06693076
Benchmarks in Acute Laparoscopic Cholecystectomy
December 26, 2024 updated by: Ebba Kihlstedt Pasquier, Region Östergötland
Benchmarks in Acute Laparoscopic Cholecystectomy - a National Registry Study
The aim of this observational cohort study is to define peri- and postoperative reference values for acute laparoscopic cholecystectomy, using the achievable benchmarks of care methodology (ABC™).
Another aim is to develop adjusted reference values for groups with a risk factor of severe postoperative complications.
The goal is to spur quality improvement initiatives.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The data source is the Swedish patient registry GallRiks, a prospective quality registry for gallbladder surgery and endoscopic retrograde cholangio-pancreatography (ERCP).
The time frame will be 2015-2023.
Register variables related to surgical quality will be analyzed, such as postoperative complications, perioperative adverse events, surgical duration and length of stay.
The study will analyze data for the time of surgery and up to 30 days afterwards.
As the researchers do not yet have the data available, the exact number of enrolled participants can not yet be given.
Study Type
Observational
Enrollment (Estimated)
40000
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Adults with gallbladder inflammation.
Description
Inclusion Criteria:
- adults ≥ 18 years of age
- laparoscopic acute cholecystectomy
Exclusion Criteria:
- other indications than acute cholecystitis will be excluded
- cholecystectomy due to malignancy
- other organ surgery performed at the same occasion
- previous upper gastrointestinal surgery
- single port access
- robotic surgery
- no data concerning surgical intervention
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Acute laparoscopic cholecystectomy
Patients with gallbladder inflammation.
ERCP may be involved if a gallstone is detected in the common bile duct perioperatively.
|
The intervention in this study is urgent, not elective.
The conditions for the surgery are therefore different: any time of day, the surgeon on shift, the state of the patients.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Benchmark values of acute laparoscopic cholecystectomy
Time Frame: Day of surgery
|
The study will use the ABC methodology to identify reference values of surgical duration (minutes), perioperative cholangiography, conversion to open surgery and adverse events
|
Day of surgery
|
|
Postoperative benchmark values of acute laparoscopic cholecystectomy
Time Frame: 0-30 days after surgery
|
The study will use the ABC methodology to identify reference values of postoperative variables: hospital length of stay (days), abscess/infection, bleeding, biliary leakage, readmission, reoperation
|
0-30 days after surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adjusted benchmarks for severe complications
Time Frame: 0-30 days after surgery
|
Univariable and multivariable logistic regression analysis will be performed to detect any risk factor for severe complications after acute laparoscopic cholecystectomy.
The factors to be investigated are body mass index (kg/m2), age (years), gender, smoking, cardiovascular disease, pulmonary disease, diabetes, immunosuppressive treatment, and treatment with anticoagulants.
Adjusted benchmarks will be calculated for factor(s) that in multivariable logistic regression analysis are identified as individual risk factor(s).
|
0-30 days after surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2015
Primary Completion (Actual)
December 31, 2023
Study Completion (Actual)
December 31, 2023
Study Registration Dates
First Submitted
November 14, 2024
First Submitted That Met QC Criteria
November 14, 2024
First Posted (Actual)
November 18, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 26, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-06020-02
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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