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NCT00163982 Clinical Trial

Vasoactive Peptides in Portal Pressure

Portal Hypertension Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00163982
Other study ID # AH4204
Secondary ID
Status Recruiting
Phase N/A
First received September 13, 2005
Last updated July 25, 2007

Study information
Verified date September 2005
Source Bayside Health
Contact William W Kemp, MBBS, FRACP
Phone 92762000
Email w.kemp@alfred.org.au
Is FDA regulated No
Health authority Australia: Human Research Ethics Committee
Study type Interventional

Clinical Trial Summary

This study is looking at the detection of vasoactive peptides in portal hypertension.

Recruitment information / eligibility
Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- HVPG >= 12 mmHg

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Norfloxacin

Locations
Country Name City State
Australia Alfred Hospital Melbourne Victoria

Sponsors (1)
Lead Sponsor Collaborator
Bayside Health

Country where clinical trial is conducted

Australia, 

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