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Main
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Note: This record shows only the 20 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 October 2012 |
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Main ID: |
NCT01462279 |
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Date of registration:
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25/10/2011 |
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Primary sponsor: |
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Public title:
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Effect of Thiamine on Oxygen Utilization (VO2) in Critical Illness
VO2 |
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Scientific title:
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The Effect of Thiamine on VO2 Levels in Critically Ill Patients |
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Date of first enrolment:
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September 2011 |
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Target sample size:
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20 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01462279 |
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Study type:
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Interventional |
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Study design:
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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Countries of recruitment
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United States
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Contacts
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Name:
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Katherine M Berg, 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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Beth Israel Deaconess Medical Center |
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Name:
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Michael W Donnino, 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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Beth Israel Deaconess Medical Center |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Adult patients (age > 18 years) admitted to an ICU
- Mechanically ventilated
Exclusion Criteria:
- Unstable ventilator settings during measurement of VO2
- Temp > 100 at time of VO2 measurement
- FIO2 > 60%
- Endotracheal cuff leak, chest tube, or other evident source of air leak
- Thiamine supplementation within 24 hours prior to study enrollment
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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Acute Respiratory Failure
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Intervention(s)
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Drug: Thiamine
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Primary Outcome(s)
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Improvement in VO2
[Time Frame: Baseline to 9 Hours]
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Secondary Outcome(s)
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Improvement in hemodynamics
[Time Frame: Baseline to Nine Hours]
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Secondary ID(s)
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2010P-000312
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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