Evidence map›Paper›PMID 41689066›Full record

ArticleTrials2026

Antibiotic treatment for 1 day versus 4-7 days in patients with acute cholangitis after adequate endoscopic biliary drainage (COBRA): study protocol for a randomized controlled trial.

Anouk G Overdevest, Elske Sieswerda, Sylke Haal, Johannes A Bogaards, Martine A M C Baven-Pronk, Auke Bogte, Karam S Boparai, Frank Ter Borg, Menno A Brink, Foke van Delft and 29 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05750966 (Very Short-course Versus Standard Course Antibiotic Therapy in Patients With Acute ChOlangitis After Adequate Endoscopic BiliaRy drAinage), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05750966 nacompletednot on this map

Very Short-course Versus Standard Course Antibiotic Therapy in Patients With Acute ChOlangitis After Adequate Endoscopic BiliaRy drAinage

TypeinterventionalSponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)Ran2023 to 2026Enrolled410ConditionsCholangitisArmscefrtriaxone, gentamicin, cefuroxim, ciprofloxin or other antibiotics according to local guideline (24 hours), cefrtriaxone, gentamicin, cefuroxim, ciprofloxin or other antibiotics according to local guideline (4 to 7 days)
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

39 authors.

Anouk G OverdevestDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Location University of Amsterdam, De Boelelaan 1118, Amsterdam, HZ, 1081, the Netherlands. a.overdevest@amsterdamumc.nl.ORCID http://orcid.org/0009-0007-0423-9667
Elske SieswerdaEuropean Clinical Research Alliance On Infectious Diseases (Ecraid), Utrecht, the Netherlands.
Sylke HaalDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Location University of Amsterdam, De Boelelaan 1118, Amsterdam, HZ, 1081, the Netherlands.
Johannes A BogaardsDepartment of Clinical Epidemiology and Data Science, Amsterdam UMC, Location Vrije Universiteit, Amsterdam, the Netherlands.
Martine A M C Baven-PronkDepartment of Gastroenterology and Hepatology, Groene Hart Hospital, Gouda, the Netherlands.
Auke BogteDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, the Netherlands.
Karam S BoparaiDepartment of Gastroenterology and Hepatology, Amstelland Hospital, Amstelveen, the Netherlands.
Frank Ter BorgDepartment of Gastroenterology and Hepatology, Deventer Hospital, Deventer, the Netherlands.
Menno A BrinkDepartment of Gastroenterology and Hepatology, Meander Medical Center, Amersfoort, the Netherlands.
Foke van DelftDepartment of Gastroenterology and Hepatology, Radboud University Nijmegen Medical Center, Nijmegen, the Netherlands.
Vincent K DikDepartment of Gastroenterology and Hepatology, Frisius Medical Centre, Leeuwarden, the Netherlands.
Paul FockensDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Location University of Amsterdam, De Boelelaan 1118, Amsterdam, HZ, 1081, the Netherlands.
Lennard P L GilissenDepartment of Gastroenterology and Hepatology, Catharina Hospital, Eindhoven, the Netherlands.
Muhammed HadithiDepartment of Gastroenterology and Hepatology, Maasstad Hospital, Rotterdam, the Netherlands.
Wouter L HazenDepartment of Gastroenterology and Hepatology, Elisabeth-TweeSteden Hospital, Tilburg, the Netherlands.
Frans van der HeideDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, Groningen, the Netherlands.
Wouter J den HollanderDepartment of Gastroenterology and Hepatology, Alrijne Hospital, Leiderdorp, the Netherlands.
Akin IndersonDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, the Netherlands.
Pieter Jan F de JongeDepartment of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Sjoerd D KuikenDepartment of Gastroenterology and Hepatology, Onze Lieve Vrouwe Gasthuis, Amsterdam, the Netherlands.
J Marius MunnekeDepartment of Gastroenterology and Hepatology, Flevo Hospital, Almere, the Netherlands.
Lars E PerkDepartment of Gastroenterology and Hepatology, Haaglanden Medical Center, The Hague, the Netherlands.
Alexander C PoenDepartment of Gastroenterology and Hepatology, Isala Clinics, Zwolle, the Netherlands.
Jan-Werner PoleyDepartment of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, the Netherlands.
Rutger QuispelDepartment of Gastroenterology and Hepatology, Reinier de Graaf Gasthuis, Delft, the Netherlands.
Robert C H SchefferDepartment of Gastroenterology and Hepatology, Jeroen Bosch Hospital, Den Bosch, the Netherlands.
Dirk W SchölvinckDepartment of Gastroenterology and Hepatology, Zaans Medical Center, Zaandam, the Netherlands.
Ellert J van SoestDepartment of Gastroenterology and Hepatology, Spaarne Hospital, Hoofddorp, the Netherlands.
Adriaan C I T L TanDepartment of Gastroenterology and Hepatology, Canisius Wilhelmina Hospital, Nijmegen, the Netherlands.
Willem J ThijsDepartment of Gastroenterology and Hepatology, Martini Hospital, Groningen, the Netherlands.
Niels G VennemanDepartment of Gastroenterology and Hepatology, Medisch Spectrum Twente, Enschede, the Netherlands.
Robert C VerdonkDepartment of Gastroenterology and Hepatology, St Antonius Hospital, Nieuwegein, the Netherlands.
Wim van de VrieDepartment of Gastroenterology and Hepatology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
Jan Maarten VrolijkDepartment of Gastroenterology and Hepatology, Rijnstate Hospital, Arnhem, the Netherlands.
Roy L J van WanrooijAmsterdam Gastroenterology Endocrinology Metabolism, Amsterdam, the Netherlands.
Pim W WeijenborgDepartment of Gastroenterology and Hepatology, Dijklander Hospital, Hoorn, the Netherlands.
Marcel G W DijkgraafDepartment of Clinical Epidemiology and Data Science, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
Jan M PrinsDepartment of Internal Medicine, Division of Infectious Diseases, Amsterdam UMC, location University of Amsterdam, Amsterdam, the Netherlands.
Rogier P VoermansDepartment of Gastroenterology and Hepatology, Amsterdam UMC, Location University of Amsterdam, De Boelelaan 1118, Amsterdam, HZ, 1081, the Netherlands. r.p.voermans@amsterdamumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute cholangitis is an infection of the biliary tract that is managed with adequate biliary drainage combined with antibiotic treatment. The international Tokyo Guidelines 2018 recommend 4 to 7 days of antibiotic treatment after adequate biliary drainage, but observational data suggest shorter treatment may be sufficient. We assessed whether 1 day of antibiotic treatment is non-inferior to 4-7 days of antibiotic treatment for acute cholangitis after adequate biliary drainage.

methodsThe COBRA-trial is a multicentre, open-label, parallel group randomized controlled non-inferiority trial with blinded outcome assessment. A total of 416 patients with acute cholangitis will be randomly assigned in a 1:1 ratio to the intervention group (1 day of antibiotic treatment after adequate biliary drainage) or to the control group (4-7 days of antibiotic treatment after adequate biliary drainage). Patients with acute cholangitis due to common bile duct stones, benign or malignant distal biliary obstruction, or distal biliary stent dysfunction are eligible. Randomization will take place once adequate biliary drainage is achieved by ERCP. Main exclusion criteria are concomitant pancreatitis, liver abscess, cholecystitis, and another infectious diagnosis at the time of randomization, use of systemic maintenance antibiotics, and specific immunosuppressants. Patients will be stratified for blood culture results at the time of randomization and aetiology of cholangitis. The primary endpoint is clinical cure, defined as the patient being symptom-free by day 14, with no relapse or death occurring by day 30. Secondary endpoints include 30-day and 90-day all-cause mortality, relapse of cholangitis by day 90, time from ERCP to first relapse, any other subsequent infection requiring antibiotic treatment within 90 days, duration of initial hospital stay, number of days treated with antibiotics by day 30, subsequent infections with multidrug resistant (MDR) bacteria, quality of life, and cost-effectiveness. DISCUSSION: This trial assesses whether a short course of antibiotic treatment for acute cholangitis is as safe and effective compared to a longer course of antibiotic treatment. If confirmed, the results could substantially reduce antibiotic exposure and healthcare resource utilization, thereby contributing to global efforts to minimize unnecessary antibiotic treatment.

trial registrationClinicalTrials.gov NCT05750966, registered on March 2nd, 2023.

Indexed as

Anti-Bacterial AgentsCholangiopancreatography, Endoscopic RetrogradeCholangitisDrainageAcute DiseaseDrug Administration ScheduleEquivalence Trials as TopicFemaleHumansMulticenter Studies as TopicRandomized Controlled Trials as TopicTime FactorsTreatment OutcomeAnti-Bacterial AgentsAcute cholangitisAntibiotic therapyClinical trialERCPTreatment duration

Identifiers

PMID41689066
PMCPMC13011331

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.