Examination of the informed consent process as experienced by patients who have undergone a chemoembolization radioembolization or transjugular intrahepatic portosystemic shunt (TIPS) procedure
Claire Draucker
Primary Investigator
Brief description of study
The purpose of this study is to describe the experiences of patients providing IC to undergo a de novo TIPS procedure.
Detailed description of study
The purpose of this study is to describe the experiences of patients providing IC to undergo a de novo TIPS procedure.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: chemoembolization, radioembolization, transjugular intrahepatic portosystemic shunt (TIPS) procedure
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Age: - 100 Years
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Gender: All
Inclusion Criteria
1. Age 18 years and older
2. Underwent a chemoembolization, radioembolization or de novo TIPS procedure in the prior three months
3. Participated in the IC process and signed the consent form for the TIPS procedure
4. Able to read, write, and speak English.
5. Agrees to complete the Newest Vital Sign (NVS) assessment.
Exclusion Criteria
1. Family member or healthcare representative provided consent.
2. Had a revision of the TIPS procedure
3. Had repeated chemoembolization or radioembolization procedures
4. Documented history of dementia.
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