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Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Syndrome: Comparison of Liposyn III 2 Percent With Liposyn II 20 Percent

Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Syndrome: Comparison of Liposyn III 2 Percent With Liposyn II 20 Percent

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002029
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2009-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

Weight Loss, Parenteral Nutrition, Total, AIDS-Related Opportunistic Infections, Liposyn, Acquired Immunodeficiency Syndrome

Brief summary

To compare two lipid emulsions in the long-term parenteral alimentation of patients with AIDS in relation to: Clinical effectiveness. Effect on immunologic function. Effect on HIV load as measured by p24 antigen levels. Effect on relative HIV infectivity.

Interventions

Sponsors

Abbott
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Concurrent Medication: Allowed: * Zidovudine (AZT). * All drugs used for the standard treatment of opportunistic infections. * Other drugs used for the treatment of other AIDS conditions if they have been started more than 3 months prior to study entry. Patients must have: * Diagnosis of AIDS. * Weight loss of \> 10 percent premorbid body weight. * Presenting diagnosis of either opportunistic infection or Kaposi's sarcoma. * Require home total parenteral nutrition (TPN) for a period of approximately 3 months. * Life expectancy = or \> 90 days. Prior Medication: Allowed: * Zidovudine (AZT).

Exclusion criteria

Co-existing Condition: Patients with the following conditions or symptoms are excluded: * Life expectancy \< 90 days. * Biliary stasis. * History of drug abuse. Patients with the following are excluded: * Life expectancy \< 90 days. * Biliary stasis. * History of drug abuse. Prior Medication: Excluded within 3 months of study entry: * Immunomodulators. * Experimental antiviral DT. History of drug abuse.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026