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Postoperative Vasopressor Usage: SQUEEZE

NCT03805230 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25000

Last updated 2024-04-10

No results posted yet for this study

Summary

A prospective multi-centre international observational study of postoperative vasopressor use, designed to answer the question: 'What is the proportion of patients that receive vasopressor infusions? In the management of these patients;

* Are there variations in the practice between clinicians, hospitals or countries? If yes, are they associated with clinical outcome?
* What are the health economic impacts associated with receiving vasopressors?

Conditions

  • Surgical Procedures, Operative
  • Vasopressor

Sponsors & Collaborators

  • European Society of Anaesthesiology

    lead OTHER

Principal Investigators

  • Ib Jammer, Dr · Haukeland University Hospital

  • Ben Creagh-Brown · Royal Surrey County Hospital NHS Foundation Trust

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-10-05
Primary Completion
2023-10-01
Completion
2024-03-31

Countries

  • Germany
  • Netherlands

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 NCT03805230 on ClinicalTrials.gov