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Assessing Outcome After H-graft Shunt Placement (PHTN)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Kenneth Luberice, University of South Florida
ClinicalTrials.gov Identifier:
NCT00519610
First received: August 21, 2007
Last updated: August 14, 2012
Last verified: August 2012

August 21, 2007
August 14, 2012
July 2007
Not Provided
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. [ Time Frame: 5 years ] [ Designated as safety issue: No ]
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. [ Time Frame: 5 years ]
Complete list of historical versions of study NCT00519610 on ClinicalTrials.gov Archive Site
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Assessing Outcome After H-graft Shunt Placement
A Study Assessing Patient Outcomes After Placement of H-graft Portacaval Shunts for the Treatment of Portal Hypertension

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.

Research data will be collected by accessing the Tampa General Hospital medical record charts as well as the Harbourside medical charts, and extracting the necessary research data. The charts will be reviewed for the relevant medical information in order to assess outcomes in patients having H-graft shunts placed for the treatment of portal hypertension.

Observational
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Probability Sample

Patients with portal hypertension

Portal Hypertension
Other: Chart Review
Patients' charts will be reviewed for relevant medical information.
I
Patients will have charts reviewed for relevant medical information before and after surgery to assess patient outcome after placement of H-graft shunt for the treatment of portal hypertension.
Intervention: Other: Chart Review
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
66
July 2010
Not Provided

Inclusion Criteria:

  • Patients who have had H-graft shunts placed for the treatment of portal hypertension.

Exclusion Criteria:

  • Patients under the age of 18 will not be included in this study.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00519610
105982
No
Kenneth Luberice, University of South Florida
University of South Florida
Not Provided
Principal Investigator: Alexander S Rosemurgy, MD University of South Florida
University of South Florida
August 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP