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Pre- and Post-operative TEG Indices in Patients With or Without Adenocarcinoma Undergoing Surgical Resection

NCT05517811

This study is recruiting at 2 US sites in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The investigators hypothesize that abnormalities in thromboelastography (TEG) parameters in patients with liver, pancreas, biliary, esophageal, colorectal, and lung adenocarcinoma can serve as biomarkers for oncologic disease burden, cancer recurrence and overall survival as well as thrombotic and hemorrhagic post-operative complications. The investigators further hypothesize that there is histologic pathology correlates to pre-operative TEG abnormalities, and that it identifies patients with virulent tumor biology.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Liver Cancer
  • Esophageal Cancer
  • Colorectal Cancer
  • Lung Adenocarcinoma
  • Control
  • Pancreas Cancer
  • Biliary Cancer

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 to 99 years
Sex
All
Healthy volunteers
Accepted
Sponsor
University of Colorado, Denver
Last updated on ClinicalTrials.gov
August 24, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Colorado · 2

  • University of Colorado Denver · Aurora, CO
  • UCHealth Highlands Ranch Hospital · Highlands Ranch, CO

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.