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Management of Highly Active Anti-retroviral Therapy-related Hyperlipidemia Among HIV-infected Patients in Taiwan

This study is currently recruiting participants.
Verified January 2017 by Kaohsiung Medical University Chung-Ho Memorial Hospital
Sponsor:
ClinicalTrials.gov Identifier:
NCT01697540
First Posted: October 2, 2012
Last Update Posted: April 28, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
Kaohsiung Medical University Chung-Ho Memorial Hospital
September 28, 2012
October 2, 2012
April 28, 2017
September 2012
September 2019   (Final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT01697540 on ClinicalTrials.gov Archive Site
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Management of Highly Active Anti-retroviral Therapy-related Hyperlipidemia Among HIV-infected Patients in Taiwan
Tropical Medicine Center (TMC), Kaohsiung Medicine University Hospital (KMUH)
  1. Written informed consent must be obtained before any study specific procedures are undertaken.
  2. The process of the experiment (brief describe) The patients must come back for follow during 4 to 12 weeks after starting the new therapy. The investigators will follow the patients' lipid profile and any side effects and stop the observation till 36 months after starting the new therapy. The serum level of HIV-VL, CD4, GOT, GPT, triglyceride, cholesterol, HDL-cholesterol, and LDL-cholesterol will be checked every 3 months. The patients' chart and all data will be delinked to protect the patients' right and privacy.
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Observational
Observational Model: Case-Only
Time Perspective: Prospective
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Non-Probability Sample
HIV/AIDS group
HIV
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
100
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September 2019   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • HIV-infected patients who receive HAART therapy but have metabolic side effects.
  • Age over 20 years old

Exclusion Criteria:

  • Abnormal liver function: GOT or GPT 5 times over normal upper limit
Sexes Eligible for Study: All
Child, Adult, Senior
No
Contact: Jih- jin Tsai, MD 886-7-3121101 ext 6638 jijits@cc.kmu.edu.tw
Taiwan
 
 
NCT01697540
KMUHIRB-2012-05-05(I)
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Kaohsiung Medical University Chung-Ho Memorial Hospital
Kaohsiung Medical University Chung-Ho Memorial Hospital
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Kaohsiung Medical University Chung-Ho Memorial Hospital
January 2017