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NCT05820009: VIABILITY

GORE® VIABIL® Biliary Endoprosthesis in the Treatment of Benign Biliary Strictures Secondary to Chronic Pancreatitis

Suspended NA Last updated 29 January 2024
What this trial tests

NA trial testing GORE® VIABIL® Biliary Endoprosthesis in Pancreatitis, Chronic in 133 participants. Suspended.

Timeline
1 February 2024
Primary endpoint
1 August 2026
1 August 2028

Quick facts

Lead sponsorW.L.Gore & Associates
PhaseNA
StatusSuspended
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment133
Start date1 February 2024
Primary completion1 August 2026
Estimated completion1 August 2028
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

W.L.Gore & Associates — full company profile →

Who can join

18 and older, any sex, with Pancreatitis, Chronic or Stricture; Bile Duct. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will evaluate the safety and effectiveness of the GORE® VIABIL® Biliary Endoprosthesis in the treatment of benign biliary strictures secondary to Chronic Pancreatitis (CP).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pancreatitis, Chronic

Currently open trials in the same condition.

Other W.L.Gore & Associates 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/NCT05820009.

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