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Clinical Trials/NCT01828268
NCT01828268
Unknown
Not Applicable

Metabolic Fingerprintings and Metabolic Dynamics After HIV Infection:Impact of Metabolic Changes and Anti-Retroviral Therapy, Life Style and Clinical Conditions

Sichuan Academy of Medical Sciences1 site in 1 country100 target enrollmentMarch 2013
ConditionsHIV

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV
Sponsor
Sichuan Academy of Medical Sciences
Enrollment
100
Locations
1
Primary Endpoint
Dyslipidemia
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this plot study is to find out the relationship between metabolic changes and anti-retroviral therapy (ART), life style and clinical conditions of HIV-infected patients using nuclear magnetic resonance (NMR) based systems biology approach and metabolomics methodology.

Detailed Description

Since the clinical application of anti-retroviral therapy (ART) in 1997, the life expectancy of HIV infected patients has been prolonged greatly. However,side effects of ART including metabolic abnormalities have become the main factors influencing patients' quality of life. Among which the abnormal lipid metabolism plays an important role. Meanwhile, metabolic conditions differ from patients applying to different combinations of ART drugs,life style and clinical conditions. Metabolomics can measure the dynamic metabolic responses of the body to stimuli or modifications. Using nuclear magnetic resonance (NMR) as tools can systematically analyse the process of lipid metabolism. Metabolomics fingerprinting can be defined as the complete complement of small molecule (\< 1500 Da) metabolites found in a specific cell, body fluid, organ or organism. Therefore, the study of the impact of metabolic changes and anti-retroviral therapy (ART), life style and clinical conditions is of importance in enhancing the adherence and improving the clinical outcomes of HIV infected patients.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
March 2020
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of HIV infection

Exclusion Criteria

  • Pregnancy
  • Individual who is participating in other trial(s)

Outcomes

Primary Outcomes

Dyslipidemia

Time Frame: Dyslipidemia events from admission to discharge(Up to 6 months) )

Secondary Outcomes

  • Lipoatrophy(Lipoarophy events from admission to discharge (up to 6 months))

Study Sites (1)

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