Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
48 participants
OBSERVATIONAL
2018-04-01
2021-06-01
Brief Summary
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The investigators wanted to investigate, if sodium infusions could be part of the explanation.
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Detailed Description
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Method: Consecutive patients for acute, abdominal surgery were included and observed until discharge or up to seven days postoperatively with daily sodium and phosphate balance measurements.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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acute abdominal surgery
Acute surgery for acute abdominal disease
Eligibility Criteria
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Inclusion Criteria
* ready for acute surgery
* able to understand and cooperate.
Exclusion Criteria
* renal insufficiency (p-creatinine\>400 micr mol/l)
* re-operations
* expected hospital stay \< 24 hours.
18 Years
ALL
No
Sponsors
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University of Copenhagen
OTHER
Jens Rikardt Andersen
OTHER
Responsible Party
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Jens Rikardt Andersen
Associate Professor, Primary Investigator
Principal Investigators
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jens R Andersen
Role: PRINCIPAL_INVESTIGATOR
University of Copenhagen
Locations
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Herlev University Hospital
Herlev, , Denmark
Countries
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Other Identifiers
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RLS in surgery
Identifier Type: -
Identifier Source: org_study_id
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