Relationship of Vasoactive Peptide Levels to Portal Pressure and Patient Outcomes in Patients With Hepatic Cirrhosis

NCT ID: NCT00163631

Last Updated: 2006-10-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Study Classification

OBSERVATIONAL

Brief Summary

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Investigate vasoactive medicators in portal hypertension on stored sera

Detailed Description

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Conditions

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Portal Hypertension

Study Design

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Observational Model Type

DEFINED_POPULATION

Study Time Perspective

OTHER

Eligibility Criteria

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Inclusion Criteria

* portal hypertension

Exclusion Criteria

* Nil
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bayside Health

OTHER_GOV

Sponsor Role lead

Principal Investigators

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William W Kemp, MBBS FRACP

Role: PRINCIPAL_INVESTIGATOR

The Alfred

Locations

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Alfred Hospital

Melbourne, Victoria, Australia

Site Status

Countries

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Australia

Other Identifiers

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4104

Identifier Type: -

Identifier Source: org_study_id