Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06964425

Raman Spectroscopy in the Diagnosis of Extrahepatic Cholangiocarcinoma

Led by University Hospital Olomouc · Updated on 2025-07-02

20

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

Sponsors

U

University Hospital Olomouc

Lead Sponsor

P

Palacky University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the use of Raman spectroscopy, an optical technique that analyzes scattered light to provide a molecular fingerprint of tissue, to improve the diagnosis of extrahepatic cholangiocarcinoma. This cancer is difficult to diagnose due to the limited effectiveness of imaging and tissue sampling methods. The study aims to develop a method for in vivo Raman spectroscopy during bile duct examination to enhance current diagnostic capabilities. During the procedure, a fiber-optic Raman probe is inserted through an endoscope during an endoscopic retrograde cholangiopancreatography (ERCP) session. The probe is positioned under fluoroscopic guidance within the bile duct tissue affected by cholangiocarcinoma. Raman spectroscopy measurements are taken 20 times per patient—10 times on malignant tissue and 10 times on healthy bile duct tissue. The collected data are analyzed by a specialist to identify differences in tissue characteristics. Participants provide informed consent and undergo the ERCP procedure with the Raman probe as part of their diagnostic evaluation. Researchers will compare the Raman spectra of malignant versus healthy bile duct tissue to assess diagnostic differences. The study includes safety and procedural monitoring, with the total participation duration aligning with the ERCP procedure timeline. Data collection and analysis aim to support improved diagnostic methods for this challenging cancer type.

CONDITIONS

Brief Title

Raman Spectroscopy in the Diagnosis of Extrahepatic Cholangiocarcinoma - a Pilot Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Person older than 18 years
  • Known diagnosis of extrahepatic cholangiocarcinoma
  • Indicated for endoscopic retrograde cholangiopancreatography (ERCP)
Not Eligible

You will not qualify if you...

  • Disagreement with participation in the study

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo endoscopic retrograde cholangiopancreatography (ERCP) where a fiber-optic Raman probe is inserted to measure Raman spectra of malignant and healthy bile duct tissue.

1 procedure visit (in-person)

Trial Site Locations

Total: 1 location

1

Peter Slodička

Olomouc, Olomouc Region, Czechia, 77900

Actively Recruiting

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Research Team

P

Peter Slodička, M.D.

V

Václav Ranc, Assoc. Prof.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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Published Research Related To This Trial