Status:
COMPLETED
Postoperative Vasopressor Usage: SQUEEZE
Lead Sponsor:
European Society of Anaesthesiology
Conditions:
Surgical Procedures, Operative
Vasopressor
Eligibility:
All Genders
18+ years
Brief 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? ...
Detailed Description
Postoperative hypotension is a common occurrence following major non-cardiac surgery and the use of vasopressors in the postoperative period to support blood pressure following optimisation of fluid s...
Eligibility Criteria
Inclusion
- Undergoing surgery (may be planned or unplanned)
- No plans for return home on the day of surgery, for medical reasons
- Age ≥ 18 on day of surgery
Exclusion
- Cardiac surgery
- Obstetric surgery
- Transplant surgery
- Receiving long-term infusions of vasoactive drugs, such as epoprostenol
- Mechanical circulatory support: ventricular assist device, intra-aortic balloon pump, artificial heart or similar
- Already been enrolled in Squeeze
- For Cohort B - One additional inclusion criterion:
- Receiving infusion of vasopressors that continues after the patient has left the operating room.
Key Trial Info
Start Date :
October 5 2020
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
March 31 2024
Estimated Enrollment :
25000 Patients enrolled
Trial Details
Trial ID
NCT03805230
Start Date
October 5 2020
End Date
March 31 2024
Last Update
April 10 2024
Active Locations (2)
Enter a location and click search to find clinical trials sorted by distance.
1
University Hospital Knappschaftskrankenhaus Bochum
Bochum, Germany
2
Wilhelmina Hospital Assen
Assen, Netherlands