An interventional study of Diagnostic procedures in Gallstone Disease, Ultrasonic Diagnosis and Bariatric Patients Undergoing Bariatric Surgery, sponsored by Esbjerg Hospital - University Hospital of Southern Denmark. Recruiting at 1 site in Denmark. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-02.
Sponsored by Esbjerg Hospital - University Hospital of Southern Denmark · Not applicable, Interventional, and Diagnostic
Every year, many patients undergo weight-loss (bariatric) surgery. While this surgery leads to significant and intended weight loss, it also increases the risk of developing gallstones or other gallbladder problems.
Approximately one in five patients later requires a second operation to remove the gallbladder. This type of surgery carries a higher risk of complications and reoperations compared with gallbladder surgery performed in the general population.
Preventive treatment may help reduce this risk. One option is medical treatment with Ursochol, which has been shown to lower the risk of developing gallstones after bariatric surgery. However, this treatment is only effective in patients who have not already developed gallstones before surgery.
This means patients need a reliable preoperative ultrasound examination of the gallbladder. Unfortunately, performing ultrasound can be technically challenging in patients with obesity, making it harder to detect small stones or other abnormalities.
The goal is therefore to improve the examination of the gallbladder in patients undergoing bariatric surgery in order to better identify who may benefit from preventive treatment.
The study
The investigators are comparing two types of ultrasound examination of the gallbladder:
It is of interest to find out whether the ultrasound performed during surgery finds more:
By improving detection, the investigators aim to better guide preventive treatment and reduce the need for future gallbladder surgery.
BACKGROUND AND RATIONALE
2.1 Clinical Background Bariatric surgery is an established and effective treatment for severe obesity. In Denmark, approximately 2,000 bariatric procedures are performed annually. These procedures result in significant and intended weight loss and improvement in metabolic comorbidities. However, rapid weight loss is associated with an increased risk of gallstone formation.
Gallstone disease is one of the most common postoperative complications following bariatric surgery. Approximately 10% of patients undergo cholecystectomy within two years after surgery, increasing to up to 20% within ten years. Importantly, cholecystectomy in patients who previously underwent bariatric surgery is associated with:
2.2 Preventive Treatment and Diagnostic Challenge Prophylactic treatment with ursodeoxycholic acid (Ursochol) has been shown to significantly reduce the risk of symptomatic gallstone disease in the first two years after bariatric surgery.
However:
Conventional transabdominal ultrasound (TAUS) is the standard imaging modality for gallbladder evaluation. However, in patients with severe obesity:
Thus, diagnostic uncertainty may lead to:
2.3 Rationale for Laparoscopic Ultrasound (LUS)
Laparoscopic ultrasound (LUS) allows:
Only one prior study has directly compared TAUS and LUS in this population. That study suggested higher overall pathology detection with LUS, but lacked:
Therefore, a well-designed prospective paired diagnostic study is warranted.
3.1 Primary Objective To compare the diagnostic detection rate of gallbladder pathology between transabdominal ultrasound (TAUS) and laparoscopic ultrasound (LUS) in patients undergoing bariatric surgery.
3.2 Secondary Objectives
1. Laparoscopic ultrasound detects significantly more gallbladder pathology than transabdominal ultrasound.
2. LUS has lower interobserver variability compared to TAUS.
5. STUDY DESIGN Prospective observational diagnostic comparative study with paired within-patient design.
Each participant undergoes:
All examinations are performed blinded and independently.
No randomization is performed.
No experimental interventions are introduced.
6. STUDY PROCEDURES
6.1 Preoperative Phase
Participants undergo:
6.2 Intraoperative Phase
During planned bariatric surgery:
Adds 5-10 minutes to procedure
7. STATISTICAL ANALYSIS PLAN
7.1 Primary Analysis McNemar's test for paired binary outcomes.
Significance level: 0.05 (one-sided)
Power: 90%
7.2 Sample Size Calculation Sample size was calculated for a paired binary comparison of the composite gallbladder pathology outcome between transabdominal ultrasound (TAUS) and laparoscopic ultrasound (LUS) using a one-sided McNemar test (α=0.05, power=90%). The sample size was calculated in two ways. Under one model, we assumed the detection rates of 25% for TAUS and 35% for LUS with an estimated between-modality correlation of 0.70. In the second model, we assumed discordant proportions of 0.10 (TAUSnegative / LUSpositive) and 0.01 (TAUSpositive / LUSnegative). Approximately in both models, the required sample size was 117 evaluable paired patients; allowing for 10% dropout/non-evaluable cases, we will enroll 130 patients in total.
7.3 Secondary Analyses • Interobserver agreement: Cohen's kappa
All analyses conducted in STATA.
8. ETHICAL CONSIDERATIONS
8.1 Risk Assessment Both TAUS and LUS examinations are well known diagnostic modalities without any known risk profile. The LUS procedure will add 5-10 minutes of additional surgery, which seems reasonable.
Overall, the risk of the examinations are considered minimal.
8.2 Potential Benefits • Improved diagnostic precision
Simpler ultrasound examinations
9. DATA MANAGEMENT
Registered internally at hospital
10. DISSEMINATION
Results will be:
11. FUNDING
12. EXPECTED IMPACT
If LUS demonstrates superior diagnostic performance:
This study has direct translational relevance to clinical practice.
189 studies on the registry are indexed under Cholelithiasis; 42 are open to participants now.
This study's planned enrollment of 130 is above the median of 90 across 135 interventional studies indexed under Cholelithiasis.
Browse Cholelithiasis studies →Esbjerg Hospital - University Hospital of Southern Denmark is the lead sponsor of 50 studies on the registry; 15 are open to participants now.
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Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Diagnostic Test: Diagnostic procedures
In the same patients, we will do both transabdominal and laparoscopic ultrasound
Also known as: Transabdominal ultrasound, Laparoscopic ultrasound
Gallbladder pathology (yes / no)
Composite endpoint consisting of gallstones (yes/no), slugde (yes/no), micro- lithiasis (yes/no), diffuse gallbladder wall thickness over 3 mm (yes/no).
Time frame: From preoperative ultrasound (within 31 days before surgery) to laparoscopic ultrasound during bariatric surgery
Interobserver variability
Interobserver agreement (Cohen's kappa)
Time frame: From preoperative ultrasound (within 31 days before surgery) to laparoscopic ultrasound during bariatric surgery
Plan to share: No — Individual participant data will not be shared due to national data protection regulations and institutional restrictions.
No publications or documents are linked to this record.
Started Apr 2026 (actual). Primary completion is estimated for Jun 2028, 26 months after the start.
Of 54 non-industry interventional studies with no phase under Cholelithiasis, half reached primary completion within 17 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 27. This study's planned 26 months is above that.
Counting every sponsor, half of 58 studies reached it within 15 months; a quarter within 6 and three quarters within 24.
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Esbjerg Hospital - University Hospital of Southern Denmark