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NCT04408482

Does Pancreatic Stent Decrease the Risk of Pancreatitis After Pancreatic Sphincterotomy for Difficult Cannulation?

Recruiting now NA Last updated 3 March 2026
What this trial tests

NA trial testing Biliary cannulation in Endoscopic Retrograde Cholangiopancreatography in 268 participants. Currently enrolling.

Timeline
1 August 2020
Primary endpoint
1 September 2028
1 September 2028

Quick facts

Lead sponsorHelsinki University Central Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment268
Start date1 August 2020
Primary completion1 September 2028
Estimated completion1 September 2028
Sites1 location across Finland

Drugs / interventions tested

Conditions studied

Sponsor

Helsinki University Central Hospital

Who can join

Adults 18 to 100, any sex, with Endoscopic Retrograde Cholangiopancreatography. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to compare the risk of PEP after pancreatic sphincterotomy performed for difficult cannulation in a group of patients with and in a group of patients without placement of a prophylactic pancreatic stent. The definition of difficult cannulation is defined according to the literature.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Endoscopic Retrograde Cholangiopancreatography

Currently open trials in the same condition.

Other Helsinki University Central Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04408482.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing