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

ConditionCholangitis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorHepatopancreatobiliary Surgery Institute of Gansu Province

About this trial

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.

Eligibility criteria

Qualifiers

Type Ⅰ、Ⅱ、Ⅲ、Ⅳ of Hilar Cholangiocarcinoma;

Age: 18~90 years old;

Underwent diagnostic and therapeutic ERCP;

Disqualifiers

Coagulation dysfunction(INR>1.3) or/and low peripheral blood platelet count (PLT <50x10^9/L);

Preoperative acute cholangitis;

Preoperative acute pancreatitis;

Preoperative hemobilia or hemorrhage of digestive tract;

Trial design

Treatments tested in this trial

  • Injection of 37℃ contrast agent

Treatment groups

100 Participants
are divided into 2 treatment groups