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Plastic vs Biodegradable Pancreatic Stent in Post-ERCP Pancreatitis Prevention

Primary Purpose

Biliary Tract Diseases

Status
Active
Phase
Not Applicable
Locations
Ecuador
Study Type
Interventional
Intervention
Pancreatic duct stenting with plastic stent
Pancreatic duct stenting with Biodegradable Stent
Sponsored by
Instituto Ecuatoriano de Enfermedades Digestivas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Biliary Tract Diseases focused on measuring Biliary tract diseases, pancreatic duct, stents

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient is scheduled for ERCP
  • Patient is 18 years old or older
  • Biliary tract disease presence
  • Non-manipulated pancreatic papilla
  • Written informed consent provided

Exclusion Criteria:

  • Patient not requiring pancreatic stenting during ERCP
  • Failed pancreatic stent placement
  • Patients at risk of fluid overload
  • Patients with cholangitis, sepsis, acute/flared up chronic pancreatitis
  • Recent previous biliary tract manipulation (i.e., pancreatoscopy, wirsungoscopy, etc.)
  • Hemodynamic instability
  • Uncontrolled coagulopathy, kidney/liver failure, or any comorbidity with a meaningful impact on cardiac risk assessment (NHYA III/IV)
  • Pregnancy or nursing
  • Refuse to participate in the study or to sign corresponding informed consent

Sites / Locations

  • Carlos Robles-Medranda

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Pancreatic duct stenting with plastic stent

Pancreatic duct stenting with Biodegradable Stent

Arm Description

Plastic pancreatic duct stent placement (5fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.

Biodegradable pancreatic duct stent placement (6fr x 4 cm or 6fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.

Outcomes

Primary Outcome Measures

PEP prevention at 72 hours
Determine if plastic or biodegradable pancreatic stent placement renders PEP prevention. PEP is defined as proposed by Cotton et al in 1991(new hospitalization admission or 2/3-day hospital stay extension due to an abdominal pain suggestive of pancreatitis, plus a threefold increase of serum amylase/lipase above the normal limits 24 hours post-procedure).

Secondary Outcome Measures

PEP prevention at 4 weeks
Determine if plastic or biodegradable pancreatic stent placement renders PEP prevention. PEP is defined as proposed by Cotton et al in 1991(new hospitalization admission or 2/3-day hospital stay extension due to an abdominal pain suggestive of pancreatitis, plus a threefold increase of serum amylase/lipase above the normal limits 24 hours post-procedure).

Full Information

First Posted
March 24, 2022
Last Updated
March 24, 2022
Sponsor
Instituto Ecuatoriano de Enfermedades Digestivas
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1. Study Identification

Unique Protocol Identification Number
NCT05307861
Brief Title
Plastic vs Biodegradable Pancreatic Stent in Post-ERCP Pancreatitis Prevention
Official Title
Plastic vs Biodegradable Pancreatic Stent Comparison in the Prevention of Post-ERCP Pancreatitis: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
December 30, 2022 (Anticipated)
Study Completion Date
January 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto Ecuatoriano de Enfermedades Digestivas

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Multiple risk factors have been linked with post-endoscopic retrograde cholangiopancreatography pancreatitis (PEP); therefore, it is critical to follow strategies to reduce associated risk, morbidity, and mortality. However, there are also factors, such as pancreatic duct stenting, which have shown evidence of PEP prevention. The investigators pursue to compare plastic vs biodegradable pancreatic stents in the prevention of PEP.
Detailed Description
Endoscopic retrograde cholangiopancreatography (ERCP) is a high-skilled endoscopic procedure, which is currently mainly used as a therapeutic mean for various pancreaticobiliary disorders. Its most common serious adverse event is PEP. Multiple risk factors have been linked with PEP (patient/procedure/operator-related). Therefore, it is critical to follow strategies to reduce associated risk, morbidity, and mortality. A recent metanalysis reported an overall incidence of PEP close to 10%, with an even higher incidence (14.7%) in high-risk patients. PEP's risk factors work synergically and have exhibited up to a 40% incidence rate in multifactorial patients. However, there are also factors, such as pancreatic duct stenting, which have shown evidence of PEP prevention. The prophylactic use of pancreatic duct stents (especially 5 Fr stents) has exhibited a statistically significant PEP severity and incidence reduction; particularly for high-risk patients, for those who have undergone inadvertent repeated pancreatic duct cannulation or those in whom it is difficult to perform biliary cannulation. Controversially, failed pancreatic duct placement has shown a 34.7% PEP incidence rate and is considered an independent risk factor for PEP. In the case of stent migration, stent-induced perforation may arise regardless of the type of stent used (plastic or metallic), but if no signs of peritonitis are displayed, the endoscopic approach may suffice for stent removal and tracks closure. Rarely the surgical approach is guaranteed for migrated stents in the presence of peritonitis or retroperitoneal fluid collection. The investigators pursue to compare plastic vs biodegradable pancreatic stents in the prevention of PEP.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Biliary Tract Diseases
Keywords
Biliary tract diseases, pancreatic duct, stents

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
98 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pancreatic duct stenting with plastic stent
Arm Type
Active Comparator
Arm Description
Plastic pancreatic duct stent placement (5fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.
Arm Title
Pancreatic duct stenting with Biodegradable Stent
Arm Type
Active Comparator
Arm Description
Biodegradable pancreatic duct stent placement (6fr x 4 cm or 6fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.
Intervention Type
Device
Intervention Name(s)
Pancreatic duct stenting with plastic stent
Intervention Description
Plastic pancreatic duct stent placement (5fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.
Intervention Type
Device
Intervention Name(s)
Pancreatic duct stenting with Biodegradable Stent
Intervention Description
Biodegradable pancreatic duct stent placement (6fr x 4 cm or 6fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.
Primary Outcome Measure Information:
Title
PEP prevention at 72 hours
Description
Determine if plastic or biodegradable pancreatic stent placement renders PEP prevention. PEP is defined as proposed by Cotton et al in 1991(new hospitalization admission or 2/3-day hospital stay extension due to an abdominal pain suggestive of pancreatitis, plus a threefold increase of serum amylase/lipase above the normal limits 24 hours post-procedure).
Time Frame
up to 72 hours after randomization
Secondary Outcome Measure Information:
Title
PEP prevention at 4 weeks
Description
Determine if plastic or biodegradable pancreatic stent placement renders PEP prevention. PEP is defined as proposed by Cotton et al in 1991(new hospitalization admission or 2/3-day hospital stay extension due to an abdominal pain suggestive of pancreatitis, plus a threefold increase of serum amylase/lipase above the normal limits 24 hours post-procedure).
Time Frame
up to 4 weeks after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient is scheduled for ERCP Patient is 18 years old or older Biliary tract disease presence Non-manipulated pancreatic papilla Written informed consent provided Exclusion Criteria: Patient not requiring pancreatic stenting during ERCP Failed pancreatic stent placement Patients at risk of fluid overload Patients with cholangitis, sepsis, acute/flared up chronic pancreatitis Recent previous biliary tract manipulation (i.e., pancreatoscopy, wirsungoscopy, etc.) Hemodynamic instability Uncontrolled coagulopathy, kidney/liver failure, or any comorbidity with a meaningful impact on cardiac risk assessment (NHYA III/IV) Pregnancy or nursing Refuse to participate in the study or to sign corresponding informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlos Robles-Medranda
Organizational Affiliation
Ecuadorian Institute of Digestive Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
Carlos Robles-Medranda
City
Guayaquil
State/Province
Guayas
ZIP/Postal Code
090505
Country
Ecuador

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27546389
Citation
ASGE Standards of Practice Committee; Chandrasekhara V, Khashab MA, Muthusamy VR, Acosta RD, Agrawal D, Bruining DH, Eloubeidi MA, Fanelli RD, Faulx AL, Gurudu SR, Kothari S, Lightdale JR, Qumseya BJ, Shaukat A, Wang A, Wani SB, Yang J, DeWitt JM. Adverse events associated with ERCP. Gastrointest Endosc. 2017 Jan;85(1):32-47. doi: 10.1016/j.gie.2016.06.051. Epub 2016 Aug 18. No abstract available.
Results Reference
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PubMed Identifier
25088919
Citation
Kochar B, Akshintala VS, Afghani E, Elmunzer BJ, Kim KJ, Lennon AM, Khashab MA, Kalloo AN, Singh VK. Incidence, severity, and mortality of post-ERCP pancreatitis: a systematic review by using randomized, controlled trials. Gastrointest Endosc. 2015 Jan;81(1):143-149.e9. doi: 10.1016/j.gie.2014.06.045. Epub 2014 Aug 1.
Results Reference
result
PubMed Identifier
15173799
Citation
Freeman ML, Guda NM. Prevention of post-ERCP pancreatitis: a comprehensive review. Gastrointest Endosc. 2004 Jun;59(7):845-64. doi: 10.1016/s0016-5107(04)00353-0. No abstract available.
Results Reference
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PubMed Identifier
2070995
Citation
Cotton PB, Lehman G, Vennes J, Geenen JE, Russell RC, Meyers WC, Liguory C, Nickl N. Endoscopic sphincterotomy complications and their management: an attempt at consensus. Gastrointest Endosc. 1991 May-Jun;37(3):383-93. doi: 10.1016/s0016-5107(91)70740-2.
Results Reference
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PubMed Identifier
24119510
Citation
Moffatt DC, Yu BN, Yie W, Bernstein CN. Trends in utilization of diagnostic and therapeutic ERCP and cholecystectomy over the past 25 years: a population-based study. Gastrointest Endosc. 2014 Apr;79(4):615-22. doi: 10.1016/j.gie.2013.08.028. Epub 2013 Oct 8.
Results Reference
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PubMed Identifier
23612857
Citation
Mazaki T, Mado K, Masuda H, Shiono M. Prophylactic pancreatic stent placement and post-ERCP pancreatitis: an updated meta-analysis. J Gastroenterol. 2014 Feb;49(2):343-55. doi: 10.1007/s00535-013-0806-1. Epub 2013 Apr 24.
Results Reference
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PubMed Identifier
23920031
Citation
Buxbaum J, Yan A, Yeh K, Lane C, Nguyen N, Laine L. Aggressive hydration with lactated Ringer's solution reduces pancreatitis after endoscopic retrograde cholangiopancreatography. Clin Gastroenterol Hepatol. 2014 Feb;12(2):303-7.e1. doi: 10.1016/j.cgh.2013.07.026. Epub 2013 Aug 3.
Results Reference
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Citation
Anderloni A, Fugazza A, Maroni L, Ormando V, Maselli R, Carrara S, Cappello A, Mangiavillano B, Omodei P, Preatoni P, Galtieri PA, Pellegatta G, Repici A. New biliary and pancreatic biodegradable stent placement: a single-center, prospective, pilot study (with video). Gastrointest Endosc. 2020 Aug;92(2):405-411. doi: 10.1016/j.gie.2020.02.049. Epub 2020 Mar 5.
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Citation
Phillip V, Pukitis A, Epstein A, Hapfelmeier A, Haf D, Schwab M, Demir IE, Rosendahl J, Hoffmeister A, Schmid RM, Weber A, Algul H. Pancreatic stenting to prevent post-ERCP pancreatitis: a randomized multicenter trial. Endosc Int Open. 2019 Jul;7(7):E860-E868. doi: 10.1055/a-0886-6384. Epub 2019 Jul 3.
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Plastic vs Biodegradable Pancreatic Stent in Post-ERCP Pancreatitis Prevention

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