Vasoactive Peptides in Portal Pressure
This study is looking at the detection of vasoactive peptides in portal hypertension...
Brief Summary
This study is looking at the detection of vasoactive peptides in portal hypertension.
- Study Type: Interventional
- Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Intervention(s) in this Clinical Trial
- Drug: Norfloxacin
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- HVPG >= 12 mmHg
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 18 Years
Maximum Age for this Clinical Trial: 75 Years
Clinical Trial Investigator Information
Lead Investigator: Bayside Health Other
Overall Clinical Trial Officials and Contacts
William W Kemp, MBBS, FRACP Principal Investigator The Alfred
Overall Contact: William W Kemp, MBBS, FRACP 92762000 w.kemp@alfred.org.au
Additional Information
Information obtained from ClinicalTrials.gov on February 12, 2012
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00163982
Study ID Number: AH4204
ClinicalTrials.gov Identifier: NCT00163982
Health Authority: Australia: Human Research Ethics Committee
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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00163982
