Case Control Study of Non Viral Hepatitis Relating to Herbal Drug Use in the Emergency Department
NCT ID: NCT00201578
Last Updated: 2006-04-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
OBSERVATIONAL
Brief Summary
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Since there is a high prevalence in the usage of traditional Chinese herbal medicine in Taiwan, this study examines the frequency of patients using herbal medicine whose initial diagnosis in the emergency department (ED) is acute non viral hepatitis. We, the researchers at National Taiwan University Hospital, then correlate if the cause of hepatitis is related to the use of these herbal drugs by taking a detailed history of medication or herbs used and by verifying the contents by chemical analysis of the "medications" used. To our knowledge, this is the first study in examining the relationship between non viral hepatitis and the use of herbal drugs prior to arriving at the ED. We expect to prove adverse effects of these substances, especially hepatitis, is the cause for requiring emergency care.
Our study design is a prospective, density sampling case control study in which one hundred patients with non viral hepatitis will be recruited as our case. We use a questionnaire designed by the investigator in the survey of demographic background, education, and income status of the cases, as well as the frequency of use of the drug, total dosage used, where the drug was purchased, what the drug is used for, and whether they know of any adverse effect that the drug might have. If they had taken the drug within three months prior to this emergency visit, then they are asked to bring the drug in for examination. Examination of the drug includes the use of high performance liquid chromatography (HPLC) and if necessary, inductively coupled plasma mass spectrometry (ICP mass). In contrast, our control group consists of subjects that are admitted to the ED due to trauma or fracture. For each case, they are matched with two subjects in the control group in both gender and age. They should also arrive within two days after the arrival of the case. All cases and controls are screened for viral hepatitis and serology must be negative before entering the study. The questionnaire is given to both groups. If more than one control is eligible to enter the study, then the control is chosen by a random draw in a hat. After this use of density sampling, we collect the data and logistic regression is used for analysis.
Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_CONTROL
OTHER
Eligibility Criteria
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Inclusion Criteria
* Hepatitis other than viral induced
Exclusion Criteria
* Viral hepatitis
18 Years
ALL
No
Sponsors
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National Taiwan University Hospital
OTHER
Principal Investigators
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Jung D Wang
Role: STUDY_DIRECTOR
National Taiwan University
Locations
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National Taiwan University Hospital
Taipei, , Taiwan
Countries
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Facility Contacts
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Ting I Lai
Role: primary
Other Identifiers
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9361701120
Identifier Type: -
Identifier Source: org_study_id