|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | National Center for Complementary and Alternative Medicine (NCCAM) |
|---|---|
| Collaborator: |
Office of Dietary Supplements (ODS) |
| Information provided by: | National Center for Complementary and Alternative Medicine (NCCAM) |
| ClinicalTrials.gov Identifier: | NCT00069524 |
Purpose
The primary goal of this study is to evaluate the short-term safety and potential efficacy of oyster mushrooms (Pleurotus ostreatus) for treatment of hyperlipidemia in HIV-infected patients who are taking Kaletra, a protease inhibitor (PI) that is commonly used in highly active antiretroviral therapy (HAART).
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections Hyperlipidemia |
Drug: oyster mushroom |
Phase I Phase II |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Antihyperlipidemic Effects of Oyster Mushrooms |
| Estimated Enrollment: | 20 |
| Study Start Date: | June 2004 |
| Study Completion Date: | May 2006 |
This is a single-arm, open-label, 8-week "proof of concept" pilot study in 20 subjects to determine if there are detectable lipid-lowering effects of oyster mushrooms in patients with HIV and hyperlipidemia who are taking Kaletra (a ritonavir-containing HAART regimen). The study will also assess whether the concurrent administration of oyster mushrooms and such regimens is safe, and investigate the mechanism of action whereby oyster mushrooms may exert their antihyperlipidemic effect.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion criteria:
Exclusion criteria:
Contacts and Locations| United States, California | |
| General Clinical Research Center, San Francisco General Hospital | |
| San Francisco, California, United States | |
| Principal Investigator: | Donald I Abrams, MD | University of California, San Francisco |
More Information
| ClinicalTrials.gov Identifier: | NCT00069524 History of Changes |
| Other Study ID Numbers: | R21 AT001782-01 |
| Study First Received: | September 29, 2003 |
| Last Updated: | September 25, 2007 |
| Health Authority: | United States: Food and Drug Administration |
|
Highly active antiretroviral therapy (HAART) Ritonavir Oyster mushrooms |
Non-HDL cholesterol Complementary Therapies Treatment Experienced |
|
HIV Infections Acquired Immunodeficiency Syndrome Hyperlipidemias Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases |
Slow Virus Diseases Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases Hypolipidemic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Lipid Regulating Agents Therapeutic Uses |