Prognostic Hemodynamic and Metabolic Profiles of Late Stage Lower Extremity Arterial Disease

NCT04143386 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2019-10-29

No results posted yet for this study

Summary

Late stage lower extremity arterial disease (LEAD) is known to be associated with hemodynamic and metabolic abnormalities and very poor long-term prognosis. The prognostic value of hemodynamic and metabolic profiling, however, is yet to be determined in this patient group.

Current study aims to identify novel prognostic biomarkers for better risk stratification of late stage LEAD patients. It also allows to determine associations between hemodynamic/arterial stiffness indices, low-molecular weight metabolites and other substances (e.g. mediators of inflammation and bone-mineral metabolism, cardiac and kidney injury biomarkers, microRNAs) thus providing potentially valuable insight into the pathogenic mechanisms of this disease.

Conditions

  • Lower Extremity Arterial Disease (Fontaine Stages IIb-IV)

Sponsors & Collaborators

  • Estonian Science Foundation

    collaborator OTHER_GOV
  • Tartu University Hospital

    collaborator OTHER
  • University of Tartu

    lead OTHER

Principal Investigators

  • Jaak Kals, MD, PhD · University of Tartu

  • Jaan Eha, MD, PhD · University of Tartu

  • Mihkel Zilmer, dr. med. · University of Tartu

  • Kaido Paapstel, MD, PhD · University of Tartu

  • Kaspar Tootsi, MD, PhD · University of Tartu

  • Karl Kuusik, MD · University of Tartu

  • Tuljo Ööbik, MD · University of Tartu

  • Riina Kaur · University of Tartu

Eligibility

Min Age
35 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-04
Primary Completion
2024-12-31
Completion
2025-12-31

Countries

  • Estonia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04143386 on ClinicalTrials.gov