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Ultrasound-guided Percutaneous Biliary Drainage Versus Endoscopic Ultrasound-guided Biliary Drainage (PUMa)

Primary Purpose

Bile Duct Obstruction, Extrahepatic

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
US-guided percutaneous biliary drainage
EUS-guided biliary drainage
Sponsored by
Theresienkrankenhaus und St. Hedwig-Klinik GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bile Duct Obstruction, Extrahepatic focused on measuring ultrasound-guided percutaneous transhepatic biliary drainage, endoscopic ultrasound-guided antegrade biliary drainage, endoscopic ultrasound-guided transhepatic biliary drainage, endoscopic ultrasound-guided choledochal biliary drainage, self-expandable metal stent, malignant bile duct obstruction

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Inoperable, malignant disease with extrahepatic bile duct obstruction (infra- hilar)
  • ERCP was not successful or wasn´t possible due to anatomical reasons (for example status post-gastrectomy)
  • At least twofold elevated bilirubin level (> 2mg/dl)
  • Histologically verified malignant disease
  • Abdominal ultrasound was performed
  • Computed tomography or magnetic resonance imaging of the abdomen was performed
  • A written consent was given

Exclusion Criteria:

  • Relevant blood coagulation disorder (Quick < 50%, Partial thromboplastin time > 50 sec., thrombocytes < 50/nl)
  • Extrahepatic cholangiocellular carcinoma (Klatskin tumor) Bismuth II-IV or intrahepatic cholangiocellular carcinoma
  • Operable, malignant disease or disease which can be cured by chemotherapy (for example aggressive Non Hodgkin-lymphoma)
  • Pregnancy or breastfeeding
  • Participation in another trial concerning PTBD or EUBD

Sites / Locations

  • Tertiary referral hospital: Theresienkrankenhaus und St. Hedwig HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

US-guided percutaneous biliary drainage

EUS-guided biliary drainage

Arm Description

The initial percutaneous transhepatic puncture of the bile duct is performed by ultrasound guidance with a Chiba-needle (0.7 mm). After injection of a radiopaque contrast media into the bile duct system, the malignant extrahepatic bile duct stenosis can be visualized by fluoroscopic guidance (digital remote-controlled fluoroscopy device). Then a 0.018 inch guide wire is introduced and proceeded beyond the tumor stenosis into the duodenum. Next, the Chiba needle is exchanged by a 5 F catheter and the 0.018 inch guide wire is exchanged by a 0.035 inch guide wire. After dilatation of the hepatic access route with bougies up to 12 F, a self-expandable metal stent is introduced. The placement of the metal stent is controlled by endoscopic luminal guidance (gastroscope or duodenoscope).

The initial transluminal puncture of the bile duct is performed by endoscopic ultrasound guidance (longitudinal echoendoscope) with an 19 G access needle. After injection of a radiopaque contrast media into the bile duct system, the malignant extrahepatic bile duct stenosis can be visualized by fluoroscopic guidance. Then, a 0.035 inch guide wire is introduced into the bile duct. After dilatation of the transluminal access route with a balloon catheter, a self-expandable metal stent is introduced as an antegrade biliary drainage, a transhepatic biliary drainage or a choledochal biliary drainage. The placement of the metal stent is controlled by fluoroscopic and endoscopic luminal guidance.

Outcomes

Primary Outcome Measures

Technical success
Successful implantation of a self-expanding metal stent to drain the obstructed bile duct, measured by the successful drainage of the radiocontrast agent by the metal stent

Secondary Outcome Measures

Clinical success
Decrease of bilirubin level on more than a half of the initial value
Adverse events
All adverse events caused by the intervention
Re-interventions
Number of re-interventions (PTBD or EUBD) that are necessary in the follow up (for example due to due stent occlusion or stent migration) after successful stent implantation
Duration of the procedure
Duration of biliary drainage procedure (US-guided percutaneous biliary drainage or EUS-guided biliary drainage) in minutes
Length of hospital stay
Length of hospital stay from the day of the first intervention (PTBD or EUBD) to the the day of discharge (days)
Survival time
Time from the day of intervention to the death of the patient

Full Information

First Posted
March 15, 2018
Last Updated
August 27, 2023
Sponsor
Theresienkrankenhaus und St. Hedwig-Klinik GmbH
Collaborators
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT03546049
Brief Title
Ultrasound-guided Percutaneous Biliary Drainage Versus Endoscopic Ultrasound-guided Biliary Drainage
Acronym
PUMa
Official Title
Prospective Multi-site Study of Ultrasound-guided Percutaneous Biliary Drainage and Endoscopic Ultrasound-guided Biliary Drainage With Implantation of a Self-expanding Metal Stent in Patients With Malignant, Distal Bile Duct Obstruction
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2018 (Actual)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Theresienkrankenhaus und St. Hedwig-Klinik GmbH
Collaborators
University Hospital Heidelberg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Prospective multi-site study of ultrasound-guided percutaneous biliary drainage and endoscopic ultrasound-guided biliary drainage with implantation of a self-expanding metal stent in patients with malignant, distal bile duct obstruction (PUMa-study)
Detailed Description
In a recent systematic review and meta-analysis about the efficacy and safety of endoscopic ultrasound-guided biliary drainage (EUBD) in comparison with percutaneous transhepatic biliary drainage (PTBD), there was no difference in technical success between the two procedures, but PTBD was associated with a lower level of clinical success, a higher level of post-procedural adverse events and a higher rate of re-interventions. The authors concluded that EUBD should be favored for biliary drainage when endoscopic retrograde cholangiopancreaticography (ERCP) failed or wasn´t possible to perform due to anatomical reasons. The hypothesis of this prospective multicenter study is that PTBD wasn´t performed in an appropriate way to compare it adequately with EUBD. The following improvements should be done. First, color Doppler ultrasound-guidance for cannulating the bile duct should be used in PTBD. The transgression of blood vessels with the risk of severe intrahepatic bleedings or hemobilia can be avoided, which are common adverse events in PTBDs when it is performed by fluoroscopic guidance. Second, the access to the bile duct from the left side of the liver should be favored. The access from the right liver side causes more adverse events such as biliary effusion or pneumothorax, as well as more patient discomfort and pain. Third, implantation of the self-expanding metal stent should be performed in the first session as a one-step procedure. This has the advantage that no further re-intervention is necessary after insertion of an external or an external/internal drainage, an outcome which can cause further adverse events such as bile duct leak along the catheter, biliary ascites or catheter dislocation. Fourth, stent release should be performed under endoscopic luminal guidance. In this way, the positioning and the correct expansion of the distal tip of the metal stent can be observed directly in comparison with the stent release which is only controlled by fluoroscopic guidance. On the other hand, EUBD should be performed in its best manner (special metal stents included) with the three techniques that are usually necessary to perform a successful EUBD: EUS-guided antegrade transpapillary drainage, EUS-guided transhepatic drainage and EUS-guided choledochal drainage. The study focuses on patients with malignant distal (infra-hilar) bile duct obstruction. It is presumed that the technical and clinical success rate is equal (non-inferiority) but the adverse event rate, the number of re-interventions and the number of days of hospitalization may differ between the two interventions. An adequate number of cases (106 patients in each intervention, drop outs included) should be recruited to calculate relevant statistical differences. Furthermore, patients will be followed over six months after the intervention to calculate an estimated survival analysis (with and without palliative chemotherapy).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bile Duct Obstruction, Extrahepatic
Keywords
ultrasound-guided percutaneous transhepatic biliary drainage, endoscopic ultrasound-guided antegrade biliary drainage, endoscopic ultrasound-guided transhepatic biliary drainage, endoscopic ultrasound-guided choledochal biliary drainage, self-expandable metal stent, malignant bile duct obstruction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective, non-randomized multicenter study (each center performs the intervention which can do best)
Masking
InvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
216 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
US-guided percutaneous biliary drainage
Arm Type
Active Comparator
Arm Description
The initial percutaneous transhepatic puncture of the bile duct is performed by ultrasound guidance with a Chiba-needle (0.7 mm). After injection of a radiopaque contrast media into the bile duct system, the malignant extrahepatic bile duct stenosis can be visualized by fluoroscopic guidance (digital remote-controlled fluoroscopy device). Then a 0.018 inch guide wire is introduced and proceeded beyond the tumor stenosis into the duodenum. Next, the Chiba needle is exchanged by a 5 F catheter and the 0.018 inch guide wire is exchanged by a 0.035 inch guide wire. After dilatation of the hepatic access route with bougies up to 12 F, a self-expandable metal stent is introduced. The placement of the metal stent is controlled by endoscopic luminal guidance (gastroscope or duodenoscope).
Arm Title
EUS-guided biliary drainage
Arm Type
Experimental
Arm Description
The initial transluminal puncture of the bile duct is performed by endoscopic ultrasound guidance (longitudinal echoendoscope) with an 19 G access needle. After injection of a radiopaque contrast media into the bile duct system, the malignant extrahepatic bile duct stenosis can be visualized by fluoroscopic guidance. Then, a 0.035 inch guide wire is introduced into the bile duct. After dilatation of the transluminal access route with a balloon catheter, a self-expandable metal stent is introduced as an antegrade biliary drainage, a transhepatic biliary drainage or a choledochal biliary drainage. The placement of the metal stent is controlled by fluoroscopic and endoscopic luminal guidance.
Intervention Type
Procedure
Intervention Name(s)
US-guided percutaneous biliary drainage
Other Intervention Name(s)
WallFlex™ Biliary RX Stents Boston Scientific
Intervention Description
Device: metal stent. The self-expandable metal stent is implanted percutaneously by a transhepatic access route. The metal stent is partially covered or non-covered (in cases in which the gallbladder is not removed). Length: 6-10 cm. Diameter: 8-10 mm.
Intervention Type
Procedure
Intervention Name(s)
EUS-guided biliary drainage
Other Intervention Name(s)
WallFlex™ Biliary RX Stents Boston Scientific
Intervention Description
Device: metal stent. The transluminal (transgastric, transduodenal or transenteric) implanted self-expandable metal stent is released via echoendoscope. The metal stent is partially covered or non-covered (in cases in which the gallbladder is not removed) or mixed covered (one half covered, one half non-covered). The mixed covered stent is used for the transhepatic access. Length: 6-10 cm. Diameter: 8-10 mm.
Primary Outcome Measure Information:
Title
Technical success
Description
Successful implantation of a self-expanding metal stent to drain the obstructed bile duct, measured by the successful drainage of the radiocontrast agent by the metal stent
Time Frame
1 minute after injection of a radiocontrast agent into the expanded metal stent
Secondary Outcome Measure Information:
Title
Clinical success
Description
Decrease of bilirubin level on more than a half of the initial value
Time Frame
7 days after the intervention
Title
Adverse events
Description
All adverse events caused by the intervention
Time Frame
Up to 30 days after the intervention
Title
Re-interventions
Description
Number of re-interventions (PTBD or EUBD) that are necessary in the follow up (for example due to due stent occlusion or stent migration) after successful stent implantation
Time Frame
6 months after successful implantation of the metal stent
Title
Duration of the procedure
Description
Duration of biliary drainage procedure (US-guided percutaneous biliary drainage or EUS-guided biliary drainage) in minutes
Time Frame
The day of the performed procedure (24 h), usually from 10 minutes up to 180 minutes
Title
Length of hospital stay
Description
Length of hospital stay from the day of the first intervention (PTBD or EUBD) to the the day of discharge (days)
Time Frame
The day of the first PTBD or EUBD is counted as day 1 of hospital stay. The day of the discharge from the hospital is counted as the last day of hospital stay. An average 7 to 14 days is estimated.y.
Title
Survival time
Description
Time from the day of intervention to the death of the patient
Time Frame
Follow up of six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Inoperable, malignant disease with extrahepatic bile duct obstruction (infra- hilar) ERCP was not successful or wasn´t possible due to anatomical reasons (for example status post-gastrectomy) At least twofold elevated bilirubin level (> 2mg/dl) Histologically verified malignant disease Abdominal ultrasound was performed Computed tomography or magnetic resonance imaging of the abdomen was performed A written consent was given Exclusion Criteria: Relevant blood coagulation disorder (Quick < 50%, Partial thromboplastin time > 50 sec., thrombocytes < 50/nl) Extrahepatic cholangiocellular carcinoma (Klatskin tumor) Bismuth II-IV or intrahepatic cholangiocellular carcinoma Operable, malignant disease or disease which can be cured by chemotherapy (for example aggressive Non Hodgkin-lymphoma) Pregnancy or breastfeeding Participation in another trial concerning PTBD or EUBD
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daniel Schmitz, Dr.med.
Phone
00496214245575
Email
d.schmitz@theresienkrankenhaus.de
First Name & Middle Initial & Last Name or Official Title & Degree
Jochen Rudi, Prof.Dr.med.
Phone
00496214244631
Email
j.rudi@theresienkrankenhaus.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anja Sander, Dr.M.Sc.
Organizational Affiliation
Institut für Medizinische Biometrie und Informatik Abteilung Medizinische Biometrie, Heidelberg University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Tertiary referral hospital: Theresienkrankenhaus und St. Hedwig Hospital
City
Mannheim
ZIP/Postal Code
68165
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daniel Schmitz, MD
Phone
00496214245575
Email
d.schmitz@theresienkrankenhaus.de
First Name & Middle Initial & Last Name & Degree
Jochen Rudi, MD PD
Phone
00496214245937
Email
j.rudi@theresienkrankenhaus.de
First Name & Middle Initial & Last Name & Degree
Daniel Schmitz, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Citation
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Results Reference
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Results Reference
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Ultrasound-guided Percutaneous Biliary Drainage Versus Endoscopic Ultrasound-guided Biliary Drainage

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