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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01582087
Other study ID # 12-030
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date February 2012
Est. completion date July 24, 2018

Study information

Verified date July 2023
Source The University of Texas Medical Branch, Galveston
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to understand mechanisms associated with the development of coma during hepatic failure. As of today, those mechanisms are not understood and it is difficult to intervene and prevent coma development which is often associated with mortality. Understanding the mechanism involved, may allow us to prevent coma and develop new therapies to treat this disease.


Recruitment information / eligibility

Status Terminated
Enrollment 11
Est. completion date July 24, 2018
Est. primary completion date July 24, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients (male or female), 18 years or older hospitalized or seen at UTMB clinics for chronic or acute hepatic failure will be included in the study. Exclusion Criteria: - Patients (male or female), 18 years or older hospitalized or seen at UTMB clinics that do not have a diagnosis of chronic or acute hepatic failure

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States The University of Texas Medical Branch Galveston Texas

Sponsors (1)

Lead Sponsor Collaborator
The University of Texas Medical Branch, Galveston

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The relationship that exist between a liver undergoing chronic or acute degeneration and hepatic coma. 8 weeks