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Sponsored by: |
Hvidovre University Hospital |
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Information provided by: | Hvidovre University Hospital |
ClinicalTrials.gov Identifier: | NCT00115947 |
The purpose of this study is to investigate the effect of terlipressin on myocardial perfusion and renal function.
Hypothesis: Significant improvement of renal function reflected by: glomerular filtration rate (GFR), renal blood flow (RBF), excretion of salt and metabolites in the urine and related hormones and peptides in the blood. No effect on the systolic function of the heart.
Condition | Intervention | Phase |
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Cirrhosis Ascites |
Drug: Terlipressin |
Phase II Phase III |
Study Type: | Interventional |
Study Design: | Randomized, Double-Blind, Placebo Control, Crossover Assignment, Efficacy Study |
Ages Eligible for Study: | 18 Years to 75 Years |
Genders Eligible for Study: | Both |
Inclusion Criteria:
Study ID Numbers: | 2004-000568-29 |
Study First Received: | June 26, 2005 |
Last Updated: | March 8, 2006 |
ClinicalTrials.gov Identifier: | NCT00115947 |
Health Authority: | Denmark: Danish Medicines Agency |
Liver Diseases Digestive System Diseases Fibrosis |
Ascites Terlipressin Liver Cirrhosis |
Pathologic Processes Therapeutic Uses Vasoconstrictor Agents |
Cardiovascular Agents Antihypertensive Agents Pharmacologic Actions |