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Clinical Trials in Czechia / NCT06807112
Starting soon Observational

The Influence of Secretin Stimulated Pancreatic Secretion on ctDNA Expression in Patients With Pancreatic Ductal Adenocarcinoma: The Role of Biomarkers in Determining the Prognosis of Pancreatic Ductal Adenocarcinoma

NCT06807112 · tracked via the Priya Life Science Czechia tracker
Phase
Observational
Started
2025-02-09
Last updated
2025-02-04

Condition(s) studied

Pancreatic AdenocarcinomaPancreatic Cancer

Investigational drug(s) / intervention(s)

Intravenously administered secretin

Intravenously administered secretin: 16 micrograms of liquid secretin will be one-time intravenously administered to patients with PDAC during the first hour of surgery. Four peripheral blood samples will then be collected. Plasmatic levels of ctDNA will be measured. Plasmatic levels of biomarkers such as mRNA, miRNA, siRNA, exoRNA, S100 proteins and amino acids, isolated from the same blood samples, will be measured and analyzed in correlation to tumor volumometry, survival rate etc. in specific intervals during follow-ups.

Study summary

The goal of this study is to assess the influence of pancreatic secretion stimulation by intravenously administered secretin on circulating tumor DNA in patients with pancreatic ductal adenocarcinoma. Additional aim of the study is to analyse a role of specific biomarkers in determining the prognosis of this disease. The main question o answer is:

Does intravenous secretin administration potentiate the release of circulating tumor DNA in patients with pancreatis ductal adenocarcinoma?

Additional question is:

Is there a biomarker specific and sensitive enough to help to predict the prognosis and the at the time status of the disease?

Participants scheduled for surgical treament due to pancreatic ductal adenocarcinoma will be included and stimulated with intravenously administered secretin, their peripheral blood samples will then be analyzed for ctDNA levels.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * patients diagnosed with pancreatic ductal adenocarcinoma * patients indicated for surgery by multidisciplinary tumor board * patients without previously administered chemotherapy * patients with previously administered chemotherapy Exclusion Criteria: * patients diagnosed with pancreatic ductal adenocarcinoma, at the time indicated for different than surgical therapy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Surgery, Military University Hospital in Prague Prague Czechia

More Charles University, Czech Republic trials in Czechia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06807112 on ClinicalTrials.gov ↗ ← All trials in Czechia