Alcohol-related Liver Disease Clinical Trial
Official title:
Alcohol Biomarkers in Post-Liver Transplant Patients
NCT number | NCT01812226 |
Other study ID # | STU31235 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 2013 |
Est. completion date | October 2015 |
Verified date | February 2023 |
Source | Northwestern University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this study is to compare the predictive validity and reliability of PEth testing at detecting alcohol use in post liver transplant patients. A prospective cohort study will be used to test the primary hypothesis. Subjects enrolled in the study will be followed for 12 months with biomarker levels drawn at baseline, six and 12 months. The baseline interview will inquire about the previous 30 day alcohol and tobacco use; lifetime and 12 month Diagnostic and Statistical Manual-IV criteria for alcohol abuse and/or dependence; prior alcohol treatment; history of abstinence prior to transplant; co-morbid medical issues; and depression. The six and 12 months interview will focus on previous 30 day alcohol use. The baseline, six and 12 months interviews will be conducted face-to-face at each site. While many patients who receive a transplant do not live near the academic medical center that performed the surgery patient, they normally have a transplant clinic visit 1-2 times per year. Medical records and transplant databases will be assessed to assess the other variables of interest.
Status | Completed |
Enrollment | 214 |
Est. completion date | October 2015 |
Est. primary completion date | October 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - men and women 18 years and over - Participant must have received a liver transplant after January 1, 2003 - Participant must be six months or more post-transplant - Mini-mental status score of greater than or equal to 20 - Participant must be well enough to participate in the research procedures over a 12 month period - Participant must continue to be followed by the transplant center Exclusion Criteria: - Individuals who do not consent |
Country | Name | City | State |
---|---|---|---|
United States | Northwestern Memorial Hospital | Chicago | Illinois |
United States | University of Wisconsin, Madison | Madison | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Northwestern University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | specificity of PEth to detect alcohol use among post-transplant patients | The criteria standard on which we will base the specificity will be a combination of patient self-report, family member report and clinician/medical record data.
Subjects in whom any concern of current alcohol use, from any of these sources, would be considered a positive for current drinking. The PEth levels would then be compared to this standard of current alcohol use Data from previous research suggests PEth has a specificity close to 100% |
12 month follow up |
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