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Sponsored by: |
Bayside Health |
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Information provided by: | Bayside Health |
ClinicalTrials.gov Identifier: | NCT00163982 |
This study is looking at the detection of vasoactive peptides in portal hypertension.
Condition | Intervention |
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Portal Hypertension |
Drug: Norfloxacin |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Safety/Efficacy Study |
Ages Eligible for Study: | 18 Years to 75 Years |
Genders Eligible for Study: | Both |
Inclusion Criteria:
Contact: William W Kemp, MBBS, FRACP | 92762000 ext 3327 | w.kemp@alfred.org.au |
Australia, Victoria | |
Alfred Hospital | Recruiting |
Melbourne, Victoria, Australia, 3181 | |
Contact: William W Kemp, MBBS, FRACP 92762000 ext 3327 w.kemp@alfred.org.au |
Principal Investigator: | William W Kemp, MBBS, FRACP | The Alfred |
Study ID Numbers: | AH4204 |
Study First Received: | September 13, 2005 |
Last Updated: | July 25, 2007 |
ClinicalTrials.gov Identifier: | NCT00163982 History of Changes |
Health Authority: | Australia: Human Research Ethics Committee |
HVPG > 12 mmHg |
Anti-Infective Agents Anti-Bacterial Agents Norfloxacin Liver Diseases Digestive System Diseases |
Portal Hypertension Vascular Diseases Hypertension, Portal Hypertension |
Anti-Infective Agents Liver Diseases Norfloxacin Molecular Mechanisms of Pharmacological Action Vascular Diseases Enzyme Inhibitors Hypertension, Portal |
Pharmacologic Actions Anti-Bacterial Agents Digestive System Diseases Therapeutic Uses Cardiovascular Diseases Nucleic Acid Synthesis Inhibitors Hypertension |