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Common Bile Duct StonesNCT07640204

Endoscopic Retrograde Cholangiopancreatography Access and Complication Rates After Cholecystectomy With Common Bile Duct Stones

An observational study of Common Bile Duct Stones, run by Karolinska Institutet.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The aim of this retrospective, register-based study is to investigate whether access, or no access, to endoscopic retrograde cholangiopancreatography (ERCP) at a surgical unit is associated with the risk of complications in patients undergoing laparoscopic cholecystectomy with common bile duct stones detected on… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Common Bile Duct Stones
What is being tested?
Exposed group
How many people
10,000 participants
Where
No sites listed yet
Study dates
1 Aug 2026to 1 Apr 2029
How long will I take part?
30 Days
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients, ≥18 years old, undergoing laparoscopic cholecystectomy with common bile duct stones detected on intraoperative cholangiography in Sweden 2015-2025 and registered in GallRiks.

Who may be able to join

  • ≥18 years old
  • Laparoscopic cholecystectomy with common bile duct stones (CBDS) detected on intraoperative cholangiography (IOC)
  • Procedure registered in the Swedish Registry for Gallstone Surgery and ERCP (GallRiks) 2015-2025

Who cannot join

  • Open surgery
  • Conversion to open surgery
  • Transgastric ERCP

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Sara Johansson contact

+46727362315

snnsjohan@gmail.com

About this study

Official title: Complication Rates Associated With Access or Not to Endoscopic Retrograde Cholangiopancreatography (ERCP) in Units Performing Cholecystectomy, When Common Bile Duct Stones Are Detected on Intraoperative Cholangiography

The aim of this retrospective, register-based study is to investigate whether access, or no access, to endoscopic retrograde cholangiopancreatography (ERCP) at a surgical unit is associated with the risk of complications in patients undergoing laparoscopic cholecystectomy with common bile duct stones detected on intraoperative cholangiography.

Read the detailed description

Annually, approximately 15,000 cholecystectomies are performed in Sweden. Cholecystectomy is indicated if gallstones cause recurrent biliary colic or complications. Gallstones can pass from the gallbladder into the common bile duct. Common bile duct stones (CBDS) can potentially cause biliary obstruction, cholangitis and pancreatitis.

Intraoperative cholangiography (IOC) during cholecystectomy is performed as a standard in Swedish surgical units. The arguments for routine IOC are several; routine IOC is associated with reduced risk of bile duct injury in patients with previous or ongoing cholecystitis, early detection of bile duct injury has been suggested to improve survival, and CBDS found by IOC, even small ones <4 mm, are associated with increased risk of complications and need for unplanned endoscopic retrograde cholangiopancreatography (ERCP) if no effort is made to clear the common bile duct.

American guidelines suggest performing IOC as a routine in adult patients undergoing laparoscopic cholecystectomy. Many countries do not practice routine IOC because it prolongs cholecystectomy and the evidence supporting its use is considered insufficient. European guidelines do not include routine IOC as a recommendation. On the other hand, both American and European guidelines advocate treatment of all CBDS, symptomatic or not.

CBDS represent a well-recognized clinical dilemma, especially when encountered first on IOC during cholecystectomy. In those situations, intraoperative treatment of CBDS has not been planned in advance.

There are several different approaches to remove CBDS. Worldwide, the two most common methods used are preoperative endoscopic retrograde cholangiopancreatography (ERCP) followed by cholecystectomy, or laparoscopic exploration of the common bile duct during cholecystectomy. In Sweden, the predominant treatment strategy for CBDS encountered on IOC is intraoperative ERCP.

The ERCP procedure itself is associated with a non-negligible risk of complications. The most common, and potentially severe, complication is post-ERCP pancreatitis (PEP). According to observational studies based on data from the Swedish Registry for Gallstone Surgery and ERCP (GallRiks), rendezvous-ERCP is associated with less complications, mainly PEP, compared to postoperative rendezvous-ERCP, and rendezvous-ERCP reduces the risk of PEP compared to conventional ERCP.

There are major differences between Swedish regions in the treatment of gallstone disease and outcome, probably because of different local routines. All units in Sweden performing cholecystectomies must be able to handle CBDS encountered at IOC, according to the national guidelines. The same guidelines advocate intraoperative ERCP with the rendezvous technique. ERCP volumes differ greatly between different surgical units in Sweden and the proportion of units performing ERCP has decreased over time. Smaller volumes of ERCP per surgeon are associated with more complications, including PEP.

In Sweden, part of the gallbladder surgery has moved from emergency care hospitals to elective, and sometimes private units, over the last few decades. Some of these units lack the equipment or expertise necessary for ERCP. Thus, despite what current national guidelines recommend, patients undergoing cholecystectomy, with a finding of CBDS on IOC, do not have the option to be treated with intra- or postoperative ERCP in such a surgical unit. Their CBDS must be treated in another way intraoperatively or with postponed ERCP after transfer to another unit.

How these structural differences in ERCP access at cholecystectomy affect the type of treatment of CBDS, time to treatment of CBDS, and thus complications, is not investigated. Because alternative treatment strategies to ERCP are used in units without access to ERCP, but also in units with access to ERCP, this question cannot simply be answered by the difference in complications from intra- and postoperative ERCP. Furthermore, these other strategies do not necessarily have a higher risk of complications compared to ERCP.

In a previous study, based on data from GallRiks, laparoscopic cholecystectomy with intraoperative rendezvous ERCP was associated with more complications compared to laparoscopic cholecystectomy with transcystic stent and postoperative ERCP.

The intention is to study how access to ERCP in different units affect complication rates in patients undergoing cholecystectomy when CBDS are detected on IOC. If the study shows no difference in risk of complications, there is a future possibility to transfer more gallbladder surgery out of emergency care hospitals and to enable more capacity for emergency surgery. On the other hand, if the study shows an increased risk of complications if the procedure is performed in a surgical unit without access to ERCP, there is an argument to transfer patients the other way around or establish capacity for ERCP at a greater number of hospitals.

Research question In patients undergoing laparoscopic cholecystectomy with CBDS on IOC, is there a difference in complication rates depending on access or not to ERCP at the surgical unit?

Aim and hypothesis The aim of this retrospective, register-based study is to investigate whether access, or no access, to ERCP at a surgical unit is associated with the risk of complications in patients undergoing laparoscopic cholecystectomy with CBDS detected on IOC.

The hypothesis is that laparoscopic cholecystectomy with CBDS on IOC in units with access to ERCP will be associated with less complications compared to units without access to ERCP.

PICO P Patients, ≥18 years old, undergoing laparoscopic cholecystectomy with CBDS detected on IOC in Sweden 2015-2025 and registered in GallRiks.

I There is no specific intervention performed in each group. Instead, patients undergoing cholecystectomy at a unit without access to ERCP are considered as exposed individuals.

C Patients undergoing cholecystectomy at a unit with access to ERCP are considered unexposed, serving as controls.

O Primary outcome is complications within 30 days. Complications from both the cholecystectomy and the ERCP, if performed, will be considered since the entire course of care is important from a safety perspective.

Data will be analyzed separately for acute and elective gallbladder procedures, as units without access to ERCP perform elective surgery to a very large extent.

Sweden has a distinctive approach to manage CBDS, and a nationwide register for gallbladder surgery and ERCP, GallRiks. When validated, GallRiks has shown high completeness and high correctness of entered data. Taken together, this provides a unique possibility to contribute to research in gallbladder surgery.

Primary outcome Complications

Secondary outcomes Length of hospital stay, time from surgery to first treatment of common bile duct stones, unplanned ERCP after surgery due to CBDS, mortality

Being tested
Exposed group
Keywords
Common bile duct stones, ERCP

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Exposed groupOther

    The exposed group consists of patients undergoing laparoscopic and diagnosed with CBDS during cholecystectomy at a unit where ERCP is not available.

Study groups in NCT07640204
Study groupRoleWhat they receive
Cholecystectomy without access to endoscopic retrograde cholangiopancreatography (ERCP)Patients, ≥18 years old, undergoing laparoscopic cholecystectomy with CBDS detected on IOC in Sweden 2015-2025 and registered in GallRiks. The cholecystectomy is performed in a unit without access to ERCP.
Receives: Other: Exposed group
Cholecystectomy with access to ERCPPatients, ≥18 years old, undergoing laparoscopic cholecystectomy with CBDS detected on IOC in Sweden 2015-2025 and registered in GallRiks. The cholecystectomy is performed in a unit with access to ERCP.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Complications

    Overall complications from both the cholecystectomy and the endoscopic retrograde cholangiopancreatography (ERCP).

    Measured: 0- 30 days from the cholecystectomy, 0-30 days from any performed ERCP

Secondary outcomes (5)
  1. Length of hospital stay

    Length of hospital stay for cholecystecomy plus ERCP

    Measured: 0-100 days from the cholecystectomy, 0-100 days from any performed ERCP

  2. Time from cholecystectomy to first treatment of common bile duct stones

    Time from cholecystectomy to first treatment of common bile duct stones (days)

    Measured: 0-100 days from the cholecystectomy

  3. Unplanned ERCP after surgery due to CBDS

    Unplanned ERCP after treatment of CBDS

    Measured: 1-365 days

  4. Unplanned readmission

    Unplanned readmission (yes or no)

    Measured: 0- 30 days from the cholecystectomy, 0-30 days from any performed ERCP

  5. Mortality

    Mortality

    Measured: 0-30 days from the cholecystectomy, 0-30 days from any performed ERCP

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Jun 2026
  2. Study start1 Aug 2026 (estimated)
  3. Primary completion1 Oct 2026 (estimated)
  4. Study completion1 Apr 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
10,000 participants (estimated)
Target duration
30 Days
IDs, dates and publications
ClinicalTrials.gov ID
NCT07640204
Sponsor's protocol ID
2026-02132-01
Status last verified
Jun 2026
First submitted
21 May 2026
Last updated
10 Jun 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Rystedt J, Montgomery A, Persson G. Completeness and correctness of cholecystectomy data in a national register--GallRiks. Scand J Surg. 2014 Dec;103(4):237-44. doi: 10.1177/1457496914523412. Epub 2014 Apr 15.

    PubMed 24737852
  • Johansson S, Runfors C, Sandblom G, Lindkvist B, Thorell A, Reuterwall Hansson M. Laparoscopic transcystic stenting with postoperative ERCP for the treatment of common bile duct stones: a safe alternative to intraoperative rendezvous ERCP-Data from the Swedish registry for gallstone surgery and ERCP (GallRiks). Surg Endosc. 2026 Apr;40(4):3040-3047. doi: 10.1007/s00464-026-12565-3. Epub 2026 Jan 21.

    PubMed 41566062
  • Syren EL, Sandblom G, Enochsson L, Eklund A, Isaksson B, Osterberg J, Eriksson S. Outcome of ERCP related to case-volume. Surg Endosc. 2022 Jul;36(7):5339-5347. doi: 10.1007/s00464-021-08915-y. Epub 2022 Jan 3.

    PubMed 34981237
  • Swahn F, Nilsson M, Arnelo U, Lohr M, Persson G, Enochsson L. Rendezvous cannulation technique reduces post-ERCP pancreatitis: a prospective nationwide study of 12,718 ERCP procedures. Am J Gastroenterol. 2013 Apr;108(4):552-9. doi: 10.1038/ajg.2012.470. Epub 2013 Feb 19.

    PubMed 23419386
  • Noel R, Arnelo U, Swahn F. Intraoperative versus postoperative rendezvous endoscopic retrograde cholangiopancreatography to treat common bile duct stones during cholecystectomy. Dig Endosc. 2019 Jan;31(1):69-76. doi: 10.1111/den.13222. Epub 2018 Jul 24.

    PubMed 29947437
  • Moller M, Gustafsson U, Rasmussen F, Persson G, Thorell A. Natural course vs interventions to clear common bile duct stones: data from the Swedish Registry for Gallstone Surgery and Endoscopic Retrograde Cholangiopancreatography (GallRiks). JAMA Surg. 2014 Oct;149(10):1008-13. doi: 10.1001/jamasurg.2014.249.

    PubMed 25133326
  • Tornqvist B, Stromberg C, Persson G, Nilsson M. Effect of intended intraoperative cholangiography and early detection of bile duct injury on survival after cholecystectomy: population based cohort study. BMJ. 2012 Oct 11;345:e6457. doi: 10.1136/bmj.e6457.

    PubMed 23060654
  • Tornqvist B, Stromberg C, Akre O, Enochsson L, Nilsson M. Selective intraoperative cholangiography and risk of bile duct injury during cholecystectomy. Br J Surg. 2015 Jul;102(8):952-8. doi: 10.1002/bjs.9832. Epub 2015 Apr 28.

    PubMed 25919401

Questions about this trial

What is this clinical trial studying?

An observational study of Common Bile Duct Stones, run by Karolinska Institutet.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 10 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sara Johansson (+46727362315, snnsjohan@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Complications (time frame: 0- 30 days from the cholecystectomy, 0-30 days from any performed ERCP). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07640204, which also lists 8 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jun 2026.

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