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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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12 December 2020 |
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Main ID: |
NCT02485457 |
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Date of registration:
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26/06/2015 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Validation of Nicom Device to Measure Stoke Volume Variation
NICOM-VAL |
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Scientific title:
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Validation of NICOM for the Detection of Modification of Stroke Volume |
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Date of first enrolment:
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June 28, 2015 |
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Target sample size:
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2 |
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Recruitment status: |
Terminated |
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URL:
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https://clinicaltrials.gov/show/NCT02485457 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Diagnostic. Masking: Single (Participant).
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Phase:
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N/A
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Countries of recruitment
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France
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- patients undergoing general anesthesia with an expected duration exceeding two hours
- gastrointestinal surgery, urological or gynecological surgery.
Exclusion Criteria:
- Difficulty of venous access.
- Contraindication for the use of oesophageal Doppler
- Contraindication for the use of Nicom
- Contraindication for the use of bispectral index
- Pregnant or lactating women
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Anesthesia
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Intervention(s)
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Drug: Ringer solution
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Procedure: Volume loading
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Primary Outcome(s)
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Stroke volume variation
[Time Frame: 6 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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