Hospital Universitari de Bellvitge
L'Hospitalet de Llobregat, Barcelona, 08907, Spain
NCT Number: NCT06375954
The aim of this clinical trial is to evaluate temporal delay (days) between biliary drainage (EUS-CDS vs ERCP as first line therapy) and chemotherapy start in patients with borderline distal malignant biliary obstruction.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
L'Hospitalet de Llobregat, Barcelona, 08907, Spain
Ecoendoscopy-guided choledochoduodenostomy (EUS-CDS) has been extended as a second line treatment in cases of ERCP failure in malignant distal biliary obstruction (MDBO). However, there are clinical trials which have compared it with ERCP as a first line treatment for MDBO in palliative patients, showing similar clinical and technical success and adverse events (AEs) rate between both techniques. Data about the benefit of this techique in borderline patients is still limited.
A recent retrospective study (Janet J et al, Ann Surg Oncol 2023) which included borderline patients, found that EUS-CDS group had significantly less delay (days) between biliary drainage and neoadjuvant chemotherapy start than the ERCP group with fewer endoscopy and surgery AEs.
Thus, our hypothesis is that EUS-CDS has benefits in terms of decreasing delay between biliary drainage and neoadjuvant chemotherapy start when compared to ERCP in MDBO in borderline patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Decompression of the bile duct by endoscopic aproach.
Other names: Biliary drainage
Self-expandable metallic stent (SEMS) deployment:
Lumen-apposing metal stent (LAMS) with coaxial double-pigtail plastic stent (DPPS) deployment:
Time frame: 1 day to 12 months
Number of days between intervention (T1-biliary drainage) and chemotherapy treatment start.
Time frame: day 0
ERCP group: cannulation, cholangiogram, correct deployment of SEMS
Time frame: 14 days after BD
In jaundice: decreasing > 50% of bilirrubin or normalization of bilirrubin levels 14 days after endoscopic procedure.
Time frame: 0 to 30 days after BD
Adverse events rate related to biliary drainage according to the AGREE classification
Time frame: 0 to 90 days after surgery
Adverse events rate related to surgery according to the Claiven and Dindo classification.
Time frame: 6 to 12 months
Number of days between intervention (T1-biliary drainage) and surgery
Trial opening soon.
Get NotifiedHospital Universitari de Bellvitge
Other
Endoscopic Ultrasound-Guided Biliary Drainage With Lumen-Apposing Stent vs Classical ERCP for First-line Therapy of Malignant Distal Biliary Obstruction in Borderline Disease: An Open-label, Multicenter Randomized Trial (CARPEDIEM-2 Trial)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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