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Plastic vs Biodegradable Pancreatic Stent in Post-ERCP Pancreatitis Prevention

I

Instituto Ecuatoriano de Enfermedades Digestivas

Status

Unknown

Conditions

Biliary Tract Diseases

Treatments

Device: Pancreatic duct stenting with plastic stent
Device: Pancreatic duct stenting with Biodegradable Stent

Study type

Interventional

Funder types

Other

Identifiers

NCT05307861
IECED-14022022

Details and patient eligibility

About

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.

Full 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.

Enrollment

98 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No 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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

98 participants in 2 patient groups

Pancreatic duct stenting with plastic stent
Active Comparator group
Description:
Plastic pancreatic duct stent placement (5fr x 4 cm) for patients in need of pancreatic duct stenting during ERCP.
Treatment:
Device: Pancreatic duct stenting with plastic stent
Device: Pancreatic duct stenting with Biodegradable Stent
Pancreatic duct stenting with Biodegradable Stent
Active Comparator group
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.
Treatment:
Device: Pancreatic duct stenting with plastic stent
Device: Pancreatic duct stenting with Biodegradable Stent

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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