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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.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00281710
Date of registration: 23/01/2006
Primary sponsor: Regional Hospital Holstebro
Public title: Urinary Aquaporin 2 Excretion After Methylprednisolone in Fasting Healthy Humans
Scientific title: Urinary Aquaporin 2 Excretion After Methylprednisolone in Fasting Healthy Humans
Date of first enrolment: October 2005
Target sample size: 20
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00281710
Study type:  Interventional
Study design:  Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind  
Countries of recruitment
Denmark
Contacts
Name:   Erling B Pedersen, Professor
Address: 
Telephone:
Email:
Affiliation:  Holstebro Hospital, 7500 Holstebro, Denmark
Name:   Thomas G Knudsen, MD
Address: 
Telephone:
Email:
Affiliation:  Holstebro Sygehus
Key inclusion & exclusion criteria

Inclusion Criteria:

- (1) Genders; both mal and female

- (2) Age; 18- 65 years old

- (3) BMI; below 30

- (4) Females had to bee in oral contraceptive treatment

Exclusion Criteria:

- (1) Clinical signs or history of disease in the heart, lungs, kidneys or endocrine
organs

- (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.



Age minimum: 18 Years
Age maximum: 65 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Healthy
Intervention(s)
Drug: Methylprednisolone
Primary Outcome(s)
FeNa+
u-AQP-2
Secondary Outcome(s)
Secondary ID(s)
MED.RES.HOS.2005.02.TGK
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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