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NCT Number: NCT06375954

EUS-guided CDS vs ERCP as First Line in Malignant Distal Obstruction in Borderline Disease (CARPEDIEM-2 Trial)

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitari de Bellvitge

L'Hospitalet de Llobregat, Barcelona, 08907, Spain

Location contact

Albert Garcia-Sumalla, MD

SUB_INVESTIGATOR

Alberto Alvarez, MD, pHD

PRINCIPAL_INVESTIGATOR

Antonio Rodriguez D'Jesus, MD, PhD

PRINCIPAL_INVESTIGATOR

Berta Laquente, MD, PhD

SUB_INVESTIGATOR

Carme Loras, MD, PhD

PRINCIPAL_INVESTIGATOR

Charly Guarner-Argente, MD, PhD

PRINCIPAL_INVESTIGATOR

Daniel Luna-Rodriguez, MD

SUB_INVESTIGATOR

Eduardo Redondo, MD, PhD

PRINCIPAL_INVESTIGATOR

Joan B Gornals, MD, PhD

CONTACT

[email protected]

+ 34 93 260 7682 ext. 2624

Jose Lariño, MD, PhD

PRINCIPAL_INVESTIGATOR

Jose R Aparicio, MD, PhD

PRINCIPAL_INVESTIGATOR

Juan J Vila, MD, PhD

PRINCIPAL_INVESTIGATOR

Juli Busquets, MD, PhD

SUB_INVESTIGATOR

Julia Escuer, MD

SUB_INVESTIGATOR

Julio G Velasquez-Rodriguez, MD

SUB_INVESTIGATOR

Maria Puigcerver-Mas, MD

CONTACT

[email protected]

+34 687332007

Sandra Maisterra, MD

SUB_INVESTIGATOR

VIcente Sanchiz, MD, PhD

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Malignant distal biliary obstruction diagnosed in patient considered BORDERLINE with biliary drainage indication: i) impaired hepatic enzymes (including hyperbilirubinemia) x3 times upper the superior normal value. ii) Radiologic singns of extrahepatic bile duct obstruction with presence of retrograde dilatation, of at least 12-mm axial diameter.
  • Consensual malignancy by a bilio-pancreatic multidisciplinar committe (histological confirmation is not mandatory)
  • Patient capable of understanding and/or singning the informed consent.
  • Patient who understands the type of study and will comply with all follow-up tests throughout its duration

Exclusion criteria

  • Pregnancy or lactation.
  • Severe coagulation disorder: INR > 1.5 non correctable with plasma administration and/or platelet count < 50.000/mm3.
  • Distal malignant biliary strictures in patients considered directly resectable, non-surgical, unresectable, or palliative
  • Benign or uncertain etiology of biliary strictures or strictures located proximally or in close proximity to the hilum.
  • Patients with prior biliary stents or other biliary drainages (e.g., PTCD).
  • Altered intestinal anatomy due to prior surgery that prevents or hinders papillary access (e.g., gastric bypass, Billroth II, duodenal switch, Roux-en-Y).
  • Stenosis in the antral or duodenal region that prevents access to the duodenum and reaching the papilla.
  • Situations that do not allow for upper gastrointestinal endoscopy (e.g., esophageal stricture).
  • Patients with functional diversity, who lack the capacity to understand the nature and potential consequences of the study, except when a legal representative is available.
  • Patients incapable of maintaining follow-up appointments (lack of adherence).
  • Lack of informed consent.

Treatment and study plan

Endoscopic biliary drainage

Procedure

Decompression of the bile duct by endoscopic aproach.

Other names: Biliary drainage

Self-expandable metallic stent (SEMS)

Device

Self-expandable metallic stent (SEMS) deployment:

  • Covering: Uncovered or Partially Covered. Non covered if gallbladder is present.
  • Size: 10x40mm or 10x60mm or 10x80mm.

Lumen-apposing metal stent (LAMS) and double-pigtail plastic stent (DPPS)

Device

Lumen-apposing metal stent (LAMS) with coaxial double-pigtail plastic stent (DPPS) deployment:

  • LAMS size: 6x8mm or 8x8mm. Consider 10x10mm if bile duct > 18mm.
  • DPPS size: 7Fr x 3-7cm.

Primary outcomes

  1. Delay in days between endoscopic biliary drainage and chemotherapy treatment start

    Time frame: 1 day to 12 months

    Number of days between intervention (T1-biliary drainage) and chemotherapy treatment start.

Secondary outcomes

  1. Technical success

    Time frame: day 0

    ERCP group: cannulation, cholangiogram, correct deployment of SEMS

  2. Clinical success

    Time frame: 14 days after BD

    In jaundice: decreasing > 50% of bilirrubin or normalization of bilirrubin levels 14 days after endoscopic procedure.

  3. AE - biliary drainage

    Time frame: 0 to 30 days after BD

    Adverse events rate related to biliary drainage according to the AGREE classification

  4. AE - surgery

    Time frame: 0 to 90 days after surgery

    Adverse events rate related to surgery according to the Claiven and Dindo classification.

  5. Delay in days between endoscopic biliary drainage and cephalic duodenopancreatectomy (CDP)

    Time frame: 6 to 12 months

    Number of days between intervention (T1-biliary drainage) and surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Joan B Gornals, MD,PhD

CONTACT

[email protected]

+34 932607682 ext. 2624

Maria Puigcerver-Mas, MD,

CONTACT

[email protected]

+34 687332007

Sponsors and collaborators

Lead sponsor

Hospital Universitari de Bellvitge

Other

Collaborators

  • Complejo Hospitalario Universitario de Santiago
  • Complejo Hospitalario de Navarra
  • Hospital Clínico Universitario de Valencia
  • Hospital General Universitario de Alicante
  • Hospital General Universitario de Castellón
  • Hospital Mutua de Terrassa
  • Hospital Universitario Ramon y Cajal
  • Hospital de Sant Pau
  • Hospital Álvaro Cunqueiro
  • University Hospital Virgen de las Nieves
  • University of Salamanca

Registry information

Official study title

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)

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Apr 19, 2024
Registry last updated
Apr 19, 2024

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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