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NCT03104569

Effect of 37℃ Non-ionic Contrast Agent During ERCP Procedure in Hilar Cholangiocarcinoma

Not yet recruiting NA Last updated 26 December 2025
What this trial tests

NA trial testing Injection of 37℃ contrast agent in Cholangitis in 100 participants. Not yet recruiting.

Timeline
1 April 2026
Primary endpoint
1 December 2028
1 December 2028

Quick facts

Lead sponsorHepatopancreatobiliary Surgery Institute of Gansu Province
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment100
Start date1 April 2026
Primary completion1 December 2028
Estimated completion1 December 2028
Sites3 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Hepatopancreatobiliary Surgery Institute of Gansu Province

Who can join

Adults 18 to 90, any sex, with Cholangitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine the effect of normal temperature and 37℃ non-ionic contrast agent acting on ERCP-related cholangeitis after endoscopic retrograde cholangiopancreatography (ERCP) in the treatment of hilar cholangiocarcinoma.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Cholangitis

Currently open trials in the same condition.

Other Hepatopancreatobiliary Surgery Institute of Gansu Province 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/NCT03104569.

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