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Assessing Outcome After H-graft Shunt Placement

NCT00519610 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 66

Last updated 2012-08-15

No results posted yet for this study

Summary

The objective of this study is to evaluate the pre-operative symptoms and medical history of patients with portal hypertension who have undergone placement of H-graft portacaval shunts and correlate this with patient outcomes.

Conditions

  • Portal Hypertension

Interventions

OTHER

Chart Review

Patients' charts will be reviewed for relevant medical information.

Sponsors & Collaborators

  • University of South Florida

    lead OTHER

Principal Investigators

  • Alexander S Rosemurgy, MD · University of South Florida

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Completion
2010-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00519610 on ClinicalTrials.gov