Urinary Aquaporin 2 Excretion After Methylprednisolone in Fasting Healthy Humans
NCT ID: NCT00281710
Last Updated: 2008-05-09
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
PHASE4
20 participants
INTERVENTIONAL
2005-10-31
2007-02-28
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
CROSSOVER
SINGLE
Interventions
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Methylprednisolone
Eligibility Criteria
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Inclusion Criteria
* (2) Age; 18- 65 years old
* (3) BMI; below 30
* (4) Females had to bee in oral contraceptive treatment
Exclusion Criteria
* (2) Abnormal laboratory test (blood haemoglobin, white cell count, platelets, plasma sodium, plasma potassium, plasma creatinine, plasma albumin, plasma bilirubin, plasma alanine aminotransferase, plasma cholesterol and blood glucose)
* (3) Albuminuria or glucosuria
* (4) Cancer
* (5) Arterial hypertension
* (6) Alcohol abuse
* (7) Use of tobacco
* (8) Medical treatment, except oral contraceptives
* (9) Pregnancy or breast feeding
* (10) Medicine abuse
* (11) Donation of blood less than 1 month before the study.
18 Years
65 Years
ALL
Yes
Sponsors
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Regional Hospital Holstebro
OTHER
Principal Investigators
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Erling B Pedersen, Professor
Role: STUDY_CHAIR
Holstebro Hospital, 7500 Holstebro, Denmark
Thomas G Knudsen, MD
Role: PRINCIPAL_INVESTIGATOR
Holstebro Sygehus
Locations
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Department of Medicine, Holstebro Hospital
Holstebro, , Denmark
Countries
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Other Identifiers
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MED.RES.HOS.2005.02.TGK
Identifier Type: -
Identifier Source: org_study_id