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Postoperative Vasopressor Usage: SQUEEZE (SQUEEZE)

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ClinicalTrials.gov Identifier: NCT03805230
Recruitment Status : Not yet recruiting
First Posted : January 15, 2019
Last Update Posted : January 16, 2019
Sponsor:
Information provided by (Responsible Party):
European Society of Anaesthesiology

Brief Summary:
A prospective multi-centre international observational study of postoperative vasopressor use

Condition or disease
Surgical Procedures, Operative Vasopressor

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Study Type : Observational
Estimated Enrollment : 40000 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Postoperative Vasopressor Usage : a Prospective International Observational Study (SQUEEZE)
Estimated Study Start Date : March 1, 2020
Estimated Primary Completion Date : September 30, 2020
Estimated Study Completion Date : December 31, 2020

Group/Cohort
Cohort A
all patients admitted to participating hospitals during 7 consecutive days
Cohort B
30 sequential patients with a single additional inclusion criterion



Primary Outcome Measures :
  1. Prevalence of postoperative vasopressor usage in a none cardiac surgical population. [ Time Frame: A the primary endpoint is the proportion of patients receiving vasopressor infusions that start between 1 and 24 hours postoperatively ]
    1. What proportions of patients receive infused vasopressors postoperatively?



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Adult Patients undergoing any non-cardiac surgical procedure.
Criteria

Inclusion Criteria:

  • 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 Criteria:

  • 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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03805230


Contacts
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Contact: Sylvia Daamen 003222109414 research@esahq.org
Contact: Pierre Harlet 3222105773 research@esahq.org

Sponsors and Collaborators
European Society of Anaesthesiology
Investigators
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Study Chair: Ib Jammer, Dr Haukeland University Hospital
Study Chair: Ben Creagh-Brown Royal Surrey County Hospital NHS Foundation Trust
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Responsible Party: European Society of Anaesthesiology
ClinicalTrials.gov Identifier: NCT03805230    
Other Study ID Numbers: SQUEEZE
First Posted: January 15, 2019    Key Record Dates
Last Update Posted: January 16, 2019
Last Verified: January 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Keywords provided by European Society of Anaesthesiology:
anaesthesia
Intensive Care
vasopressor