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Comparing the Effects of EST and EPBD in Patients With Acute Biliary Pancreatitis

Primary Purpose

Acute Biliary Pancreatitis

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Endoscopic papillary balloon dilation
Endoscopic sphincterotomy
Sponsored by
Kaohsiung Veterans General Hospital.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Biliary Pancreatitis focused on measuring Endoscopic sphincterotomy, Endoscopic papillary balloon dilation, Metagenomics

Eligibility Criteria

20 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Patients with age ≥ 20 years and acute biliary pancreatitis concomitant with either signs of acute cholangitis or bile duct obstruction will be enrolled in the study. They will be randomized into two treatment groups (sphincterotomy vs. balloon dilation).

Inclusion Criteria:

Patients diagnosed with acute gallstone pancreatitis and fulfill any two items from a to c, plus one item in d, and e:

  1. abdominal pain typical of pancreatitis;
  2. elevation of serum amylase and/or lipase up to three times above normal;
  3. imaging studies (abdominal ultrasound or abdominal computed tomography) showed evidence of pancreatitis
  4. common bile duct stones, acute cholangitis (Charcot's triad), total bilirubin (total bilirubin)> 4mg / dL, bile duct dilatation (diameter> 6mm with intact gallbladder, or> 10mm when the gallbladder has been removed) plus total bilirubin 1.8 ~ 4mg / dL;
  5. exclude other causes of acute pancreatitis.

Exclusion Criteria:

  • septic shock
  • serious coagulopathy (international normalized ratio 1.5, partial thromboplastin time greater than twice that of control, platelet count <50 x 1000 / Cumm)
  • malignant tumors of the biliary and pancreatic tract
  • severe cardiovascular or mental illness which can not cooperate with the exam and treatment;
  • pregnant women
  • patient who had ever received surgery or endoscopic treatment for biliopancreatic tract

Sites / Locations

  • Kaohsiung Veterans General Hospital.Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Endoscopic papillary balloon dilation

Endoscopic sphincterotomy

Arm Description

For EPBD group, after selective cannulation of the common bile duct by the catheter, cholangiography will be performed to confirm the diagnosis of bile duct pathology. A 0.025-0.035-inch guidewire will then be inserted into the bile duct through the catheter. A dilating balloon (The controlled radial expansion (CRE) balloon dilation catheter, CRE balloon 5.5 cm (centimeter) in length, 1-1.2 cm/1.2-1.5 cm/1.5-2.0 cm in diameter) will be passed via the pre-positioned guidewire into the bile duct. Using fluoroscopic and endoscopic guidance, the balloon will be inflated with contrast medium up to the optimal size and duration (normally 5min (minutes)) after the waist on the balloon disappeared according to the patients' condition and tolerance.

For EST group,endoscopic sphincterotomy(EST) will be done as large as possible with a pull type sphincterotome (The TRUEtome, Biliary sphincterotomy sphincterotome, Single-use sphincterotome CleverCut2V) Other interventions: surgical intervention, endoscopic stenting, percutaneous transhepatic cholangiogram with balloon dilation

Outcomes

Primary Outcome Measures

Complete removal of common bile duct stones
Successful bile duct clearance was defined as complete if the final cholangiogram revealed no more filling defects.

Secondary Outcome Measures

Evaluation of adverse events
Adverse events were recorded according to the definitions and grading systems from the consensus of an American Society of Gastrointestinal Endoscopy Workshop. (P. B. Cotton, G. M. Eisen, L. Aabakken et al., "A lexicon for endoscopic adverse events: report of an ASGE workshop," Gastrointestinal Endoscopy, vol. 71, no. 3, pp. 446-454, 2010.)

Full Information

First Posted
January 8, 2016
Last Updated
January 26, 2016
Sponsor
Kaohsiung Veterans General Hospital.
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1. Study Identification

Unique Protocol Identification Number
NCT02668081
Brief Title
Comparing the Effects of EST and EPBD in Patients With Acute Biliary Pancreatitis
Official Title
Prospective Randomized Study Comparing the Effects of Endoscopic Sphincterotomy (EST) and Endoscopic Papillary Balloon Dilation (EPBD) in Patients With Acute Biliary Pancreatitis (ABP)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kaohsiung Veterans General Hospital.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study compares the effect of endoscopic sphincterotomy and endoscopic papillary balloon dilation in the treatment of acute biliary pancreatitis.Participants with acute biliary pancreatitis will be randomized into either the endoscopic sphincterotomy or endoscopic papillary balloon dilation groups.Moreover, the investigators compare the results obtained from the traditional bile/blood culture and metagenomics.
Detailed Description
Early endoscopic retrograde choledocho pancreatogram with endoscopic sphincterotomy is suggested in patients with acute biliary pancreatitis to reduce complication and mortality. Retrospective study of the investigators' hospital showed that endoscopic papillary balloon dilation is safe in the treatment of acute biliary pancreatitis. However, there is no report in literature concerning about the prospective study comparing the effect of endoscopic sphincterotomy and endoscopic papillary balloon dilation in the treatment of acute biliary pancreatitis. Moreover, the presence of infective microorganisms in the biliary and/or pancreatic ducts may play important role in both the onset and outcome of acute biliary pancreatitis. Blood or bile obtained via endoscopic means is another way to know the causative bacterium/bacteria. However, it still need considerable period of time to get the result of the culture. Recently, next-generation sequencing technologies have been developed, which can facilitate the analysis of a large number of microorganisms in different environments and human body sites. 16S(a svedberg unit) ribosomal deoxyribonucleic acid sequence analysis and metagenomics are two effective DNA sequencing approaches, and both have been used to study uncultivated gut microbial communities. Aims: To study the clinical effects of endoscopic sphincterotomy and endoscopic papillary balloon dilation in acute biliary pancreatitis. To compare the results obtained from the traditional bile/blood culture and metagenomics. Methods: Beginning from Jan 2016, patients with age ≥ 20 years and acute biliary pancreatitis concomitant with either signs of acute cholangitis or bile duct obstruction will be enrolled in the study. Participants will be randomized into either the endoscopic sphincterotomy or endoscopic papillary balloon dilation groups. The treatment effects and safety of both groups will be compared. The primary endpoint is the relative successful rates of retrieval of common bile duct stones of both groups. The secondary endpoint is the frequency of use of mechanical lithotripter, other drainage procedures, complication and mortality, as well as the number of treatment sections. Besides blood culture exam, bile will be aspirated by placing a single-use, 5-French, standard catheter (after guide-wire cannulation) into the bile duct before the injection of contrast agent for endoscopic retrograde cholangiopancreaticography. Approximately 10 mL of bile will be collected and transferred in a sterile tube. Half of the bile obtained will be transported to the microbiology laboratory in blood culture bottles and in an anaerobic transport system. Bacteria will be cultured and identified according to the standard protocol used in our clinical microbiology laboratory. Another half of the bile specimen will be sending for metagenomic study. Finally, investigators will try to compare the results obtained from the traditional bile culture /blood culture and metagenomics, and to understand the effects of infective microorganisms in the biliary and/or pancreatic ducts on the acute biliary pancreatitis. In addition, investigators want to find out the best means of early and accurate diagnosis of the pathogen responsible for the infection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Biliary Pancreatitis
Keywords
Endoscopic sphincterotomy, Endoscopic papillary balloon dilation, Metagenomics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
39 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Endoscopic papillary balloon dilation
Arm Type
Experimental
Arm Description
For EPBD group, after selective cannulation of the common bile duct by the catheter, cholangiography will be performed to confirm the diagnosis of bile duct pathology. A 0.025-0.035-inch guidewire will then be inserted into the bile duct through the catheter. A dilating balloon (The controlled radial expansion (CRE) balloon dilation catheter, CRE balloon 5.5 cm (centimeter) in length, 1-1.2 cm/1.2-1.5 cm/1.5-2.0 cm in diameter) will be passed via the pre-positioned guidewire into the bile duct. Using fluoroscopic and endoscopic guidance, the balloon will be inflated with contrast medium up to the optimal size and duration (normally 5min (minutes)) after the waist on the balloon disappeared according to the patients' condition and tolerance.
Arm Title
Endoscopic sphincterotomy
Arm Type
Active Comparator
Arm Description
For EST group,endoscopic sphincterotomy(EST) will be done as large as possible with a pull type sphincterotome (The TRUEtome, Biliary sphincterotomy sphincterotome, Single-use sphincterotome CleverCut2V) Other interventions: surgical intervention, endoscopic stenting, percutaneous transhepatic cholangiogram with balloon dilation
Intervention Type
Procedure
Intervention Name(s)
Endoscopic papillary balloon dilation
Other Intervention Name(s)
EPBD
Intervention Description
treatment of endoscopic papillary balloon dilation
Intervention Type
Procedure
Intervention Name(s)
Endoscopic sphincterotomy
Other Intervention Name(s)
EST
Intervention Description
treatment of endoscopic sphincterotomy
Primary Outcome Measure Information:
Title
Complete removal of common bile duct stones
Description
Successful bile duct clearance was defined as complete if the final cholangiogram revealed no more filling defects.
Time Frame
one year
Secondary Outcome Measure Information:
Title
Evaluation of adverse events
Description
Adverse events were recorded according to the definitions and grading systems from the consensus of an American Society of Gastrointestinal Endoscopy Workshop. (P. B. Cotton, G. M. Eisen, L. Aabakken et al., "A lexicon for endoscopic adverse events: report of an ASGE workshop," Gastrointestinal Endoscopy, vol. 71, no. 3, pp. 446-454, 2010.)
Time Frame
One week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Patients with age ≥ 20 years and acute biliary pancreatitis concomitant with either signs of acute cholangitis or bile duct obstruction will be enrolled in the study. They will be randomized into two treatment groups (sphincterotomy vs. balloon dilation). Inclusion Criteria: Patients diagnosed with acute gallstone pancreatitis and fulfill any two items from a to c, plus one item in d, and e: abdominal pain typical of pancreatitis; elevation of serum amylase and/or lipase up to three times above normal; imaging studies (abdominal ultrasound or abdominal computed tomography) showed evidence of pancreatitis common bile duct stones, acute cholangitis (Charcot's triad), total bilirubin (total bilirubin)> 4mg / dL, bile duct dilatation (diameter> 6mm with intact gallbladder, or> 10mm when the gallbladder has been removed) plus total bilirubin 1.8 ~ 4mg / dL; exclude other causes of acute pancreatitis. Exclusion Criteria: septic shock serious coagulopathy (international normalized ratio 1.5, partial thromboplastin time greater than twice that of control, platelet count <50 x 1000 / Cumm) malignant tumors of the biliary and pancreatic tract severe cardiovascular or mental illness which can not cooperate with the exam and treatment; pregnant women patient who had ever received surgery or endoscopic treatment for biliopancreatic tract
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hoi Hung Chan, MD, PhD
Phone
+886-7-342-2121
Ext
2137
Email
hoihungchan@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Tzung Jiun Tsai, MD
Phone
+886-7-342-2121
Ext
2075
Email
medfungi@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hoi Hung Chan, MD, PhD
Organizational Affiliation
Kaohsiung Veterans General Hospital.
Official's Role
Study Chair
Facility Information:
Facility Name
Kaohsiung Veterans General Hospital.
City
Kaohsiung
ZIP/Postal Code
386
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hoi Hung Chan, MD, PhD
Phone
+886-7-342-2121
Ext
2137
Email
hoihungchan@gmail.com
First Name & Middle Initial & Last Name & Degree
Tzung Jiun Tsai, MD
Phone
+886-7-342-2121
Ext
2075
Email
medfungi@gmail.com

12. IPD Sharing Statement

Learn more about this trial

Comparing the Effects of EST and EPBD in Patients With Acute Biliary Pancreatitis

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