New biomarkers may sharpen cancer diagnosis in bile duct blockages
NCT ID NCT02531607
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether measuring certain substances in bile and blood can more accurately diagnose cancer in people with bile duct blockages. Researchers will compare these new tests with standard methods in 500 adults undergoing a procedure called ERCP. The goal is to find better ways to tell cancerous from non-cancerous blockages.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 500 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2014
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients scheduled for ERCP at the Center for Interventional Endoscopy (CIE)
- Ages
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19 to 95 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Screening Criteria for Potential Participants in the Study 1. Age: ≥18years old 2. Treatment: scheduled for clinical reason to undergo an ERCP at the CIE 3. Suspected of having biliary or pancreatic disease other than cancer (chronic pancreatitis, benign biliary strictures, post-liver transplant strictures, common bile duct stones, sphincter of Oddi dysfunction or suspected of having pancreatic or peri-ampullary malignancy (including pancreatic ductal adenocarcinoma, distal cholangiocarcinoma, ampullary carcinoma, duodenal, carcinoma 4. Clinical or image data suggestive of pancreatic disease or the need for gastrointestinal or pancreatic inspection. 5. Willing and mentally able to provide consent Exclusion Criteria: 1. Age: \<18years old 2. Pregnant women 3. Post-bariatric surgery, hepaticojejunostomy and Bilroth II patients undergoing ERCP. 4. Not scheduled for endoscopic procedures for clinical reasons 5. No clinical or image data suggestive of need for clinical intervention (Endoscopy) 6. Not willing or able to sign informed consent..
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AdventHealth
Orlando, Florida, 32803, United States
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