Transabdominal and Laparoscopic Ultrasound in a Bariatric Setting

May 29, 2026 updated by: Benjamin Drejer Petersen, Esbjerg Hospital - University Hospital of Southern Denmark

Transabdominal and Laparoscopic Ultrasound in a Bariatric Setting: Utility and Diagnostic Accuracy

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:

  • Standard ultrasound performed on the outside of the abdomen using a handheld probe.
  • Laparoscopic ultrasound performed during bariatric surgery using a small ultrasound probe placed inside the abdomen, typically placed on the liver near the gallbladder.

It is of interest to find out whether the ultrasound performed during surgery finds more:

  • Gallstones
  • Sludge
  • Small stones (microlithiasis)
  • Thickening of the gallbladder wall

By improving detection, the investigators aim to better guide preventive treatment and reduce the need for future gallbladder surgery.

Study Overview

Detailed Description

  1. TITLE Transabdominal and Laparoscopic Ultrasound in a Bariatric Setting
  2. 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:

    • Increased risk of surgical complications

    • Higher rates of reoperation

    • More technically complex procedures
    • Increased risk of bile duct injury In patients with Roux-en-Y gastric bypass, management of biliary tract disease is particularly challenging due to altered gastrointestinal anatomy, which complicates endoscopic access (e.g., ERCP).

    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:

    • Ursochol is only effective in patients who do not already have gallstones.

    • Therefore, accurate preoperative detection of gallstones is essential.

    Conventional transabdominal ultrasound (TAUS) is the standard imaging modality for gallbladder evaluation. However, in patients with severe obesity:

    • Ultrasound penetration is limited
    • Image quality may be reduced
    • Small stones and sludge may be overlooked
    • Sensitivity may be as low as 62-68%

    Thus, diagnostic uncertainty may lead to:

    • Under-treatment (missed stones)

    • Over-treatment (inappropriate prophylaxis)

    • Inconsistent national implementation

    2.3 Rationale for Laparoscopic Ultrasound (LUS)

    Laparoscopic ultrasound (LUS) allows:

    • Direct placement of the probe on the liver surface

    • Shorter acoustic distance

    • Higher image resolution

    • Potentially improved detection of subtle pathology

    • Fewer hospital visits for the patients prior to surgery

    Only one prior study has directly compared TAUS and LUS in this population. That study suggested higher overall pathology detection with LUS, but lacked:

    • Histological confirmation

    • Sample size justification

    • Assessment of microlithiasis
    • Gallbladder wall measurements
    • Formal evaluation of interobserver agreement within each ultrasound modality

    Therefore, a well-designed prospective paired diagnostic study is warranted.

  3. OBJECTIVES

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. To evaluate interobserver agreement within TAUS and LUS examinations
  2. To compare examination time between modalities
  3. To assess image quality
  4. HYPOTHESES

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:

  • Two independent TAUS examinations
  • Two independent LUS examinations

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:

• Two transabdominal ultrasounds

  • Performed on the same day
  • By two independent radiologists/sonographers
  • Blinded to each other's findings

6.2 Intraoperative Phase

During planned bariatric surgery:

• Two surgeons independently perform laparoscopic ultrasound

  • Probe placed directly on liver surface
  • Examinations blinded
  • 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

• Subgroup analyses (BMI strata, bariatric surgery)

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

  • Better patient selection for preventive treatment
  • Reduced need for future gallbladder surgery
  • Simpler ultrasound examinations

    9. DATA MANAGEMENT

  • Data stored in secure SharePoint research environment and REDCap Systems
  • GDPR compliant
  • Restricted access
  • Registered internally at hospital

    10. DISSEMINATION

Results will be:

• Published regardless of outcome

• Submitted to peer-reviewed journals

11. FUNDING

• Part of a PhD program

• No funding from private companies

• Additional funding sought from regional and national foundations

12. EXPECTED IMPACT

If LUS demonstrates superior diagnostic performance:

  • It may guide selective prophylactic therapy
  • It may reduce long-term gallbladder morbidity
  • It may standardize diagnostic workup

This study has direct translational relevance to clinical practice.

Study Type

Interventional

Enrollment (Estimated)

130

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

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

Yes

Description

Inclusion Criteria:

  • Age ≥18 years
  • Scheduled for bariatric surgery
  • Able to provide informed consent

Exclusion Criteria:

  • Previous cholecystectomy
  • Previous biliary surgery
  • Previous liver surgery
  • Inability to provide informed consent

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

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Ultrasound examination
In the same patients, we will do both transabdominal and laparoscopic ultrasound
Other Names:
  • Laparoscopic ultrasound
  • Transabdominal ultrasound

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gallbladder pathology (yes / no)
Time Frame: From preoperative ultrasound (within 31 days before surgery) to laparoscopic ultrasound during bariatric surgery
Composite endpoint consisting of gallstones (yes/no), slugde (yes/no), micro- lithiasis (yes/no), diffuse gallbladder wall thickness over 3 mm (yes/no).
From preoperative ultrasound (within 31 days before surgery) to laparoscopic ultrasound during bariatric surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Interobserver variability
Time Frame: From preoperative ultrasound (within 31 days before surgery) to laparoscopic ultrasound during bariatric surgery
Interobserver agreement (Cohen's kappa)
From preoperative ultrasound (within 31 days before surgery) to laparoscopic ultrasound during bariatric surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

April 1, 2026

Primary Completion (Estimated)

June 1, 2028

Study Completion (Estimated)

March 1, 2029

Study Registration Dates

First Submitted

February 25, 2026

First Submitted That Met QC Criteria

March 3, 2026

First Posted (Actual)

March 5, 2026

Study Record Updates

Last Update Posted (Actual)

June 2, 2026

Last Update Submitted That Met QC Criteria

May 29, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared due to national data protection regulations and institutional restrictions.

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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