Urotensin II and Vascular Tone in Cirrhosis

NCT ID: NCT00163995

Last Updated: 2007-07-26

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

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Brief Summary

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This study looks at the iontophoresis of urotensin II in chronic liver disease patients.

Detailed Description

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Conditions

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Liver Diseases Cirrhosis

Keywords

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Chronic Liver Disease

Study Design

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Observational Model Type

DEFINED_POPULATION

Study Time Perspective

OTHER

Interventions

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urotensin II

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Cirrhosis
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

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 RECRUITING

Countries

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Australia

Central Contacts

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William W Kemp, MBBS, FRACP

Role: CONTACT

Phone: 92762000

Email: [email protected]

Facility Contacts

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William W Kemp, MBBS, FRACP

Role: primary

Other Identifiers

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AH4004

Identifier Type: -

Identifier Source: org_study_id