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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 August 2015 |
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Main ID: |
NCT02188888 |
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Date of registration:
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10/07/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Echocardiographic and Arterial Pressure Waveform Changes After Reducing Heart Rate With Esmolol in Septic Shock Patients
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Scientific title:
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Heart Rate Reduction With Esmolol is Associated With Improved Arterial Elastance in Patients With Septic Shock. A Prospective Observational Study |
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Date of first enrolment:
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December 2013 |
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Target sample size:
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45 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02188888 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Phase:
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N/A
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Countries of recruitment
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Italy
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Contacts
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Name:
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Andrea Morelli, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Roma La Sapienza |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- septic shock criteria
- presence of heart rate > 95 bpm.
Exclusion Criteria:
- Pregnancy
- age < 18
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Septic Shock
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Tachycardia
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Intervention(s)
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Drug: esmolol
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Primary Outcome(s)
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heart rate
[Time Frame: over a period of four hours]
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Secondary Outcome(s)
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echocardiography
[Time Frame: over a period of four hours]
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static arterial elastance
[Time Frame: over a period of four hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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