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Investigation of Human Alpha-fetoprotein Genes

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National Taiwan University

Status

Unknown

Conditions

Elevated or Normal Alpha-fetoprotein Patients

Study type

Observational

Funder types

Other

Identifiers

NCT01258894
201010019R

Details and patient eligibility

About

Studies revealed that patients with hereditary persistence of AFP also had persistent abnormal AFP. Therefore, this study will recruit the patients and their family with elevated AFP (>20 ng/mL) and normal AFP patients being control groups. Then, their AFP genes extracted from the blood will be analyzed.

Full description

Abnormal AFP elevation was usually noted in liver regeneration, HCC, nonseminomatous germ cell tumors or other malignant tumors. However, some studies revealed that patients with hereditary persistence of AFP also had persistent abnormal AFP. Therefore, we study will recruit the patients and their family with elevated AFP (>20 ng/mL) and normal AFP patients being control groups. Then, their AFP genes extracted from the blood will be analyzed. The hypothesis of this study is that the mutation of AFP gene might be one of the causes of abnormal AFP.

Enrollment

300 estimated patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The patients and their family with elevated AFP (>20 ng/mL) and normal AFP patients being control groups. More than 20 years old

Exclusion criteria

  • Pregnancy

Trial contacts and locations

1

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Central trial contact

Jin Chuan Sheu, M.D. Ph.D.

Data sourced from clinicaltrials.gov

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