NCT00441272

Brief Summary

This study will determine whether pioglitazone (Actos, a drug approved to treat diabetes, can benefit HIV-infected people with fatty liver. Fatty changes of the liver (also known as steatosis) have been linked to diabetes and long-term liver damage in some patients. Pioglitazone has been shown to improve fatty liver in people without HIV; this study will see if it is beneficial for people with HIV as well. HIV-infected patients 18 years of age and older with increased fat in the liver may be eligible for this study. Screening includes a CT scan and liver biopsy (withdrawal of a small sample of liver tissue through a needle). Participants are randomly assigned to take either 45 mg of pioglitazone or placebo (sugar pill) by mouth once a day for 48 weeks. At the end of 48 weeks, all participants stop taking their medication and are followed for an additional 48 weeks to see what, if any benefits, of pioglitazone persist after treatment is stopped. In addition to taking the study medication, participants undergo the following procedures:

  • Visits to the NIH Clinical Center over a period of approximately 2 years at day 0 and weeks 2, 8, 16, 24, 32, 40, 48, 52, 72, and 96. Most visits take about 1 hour and include blood drawing for various laboratory tests.
  • Insulin clamp test at day 0 and weeks 24 and 48 to see how the body processes glucose. This test takes 4 to 6 hours and may include an overnight stay at the Clinical Center. A catheter (plastic tube) is placed in a vein in the arm to infuse insulin and another is placed in a vein on the back of the hand to draw blood samples. Blood sugar is checked frequently and glucose is given to keep blood sugar at normal values.
  • Nutrition evaluations at day 0 and weeks 24 and 48. Subjects write down all the food they eat and drink for 4 days before the visit. They meet with a nutritionist to review the food record and to complete simple measurements of body fat and shape.
  • CT scan of liver and abdomen at weeks 24, 48, 72 and 96.
  • Liver biopsy at week 48.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for phase_2 hiv-infections

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2007

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

February 27, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 28, 2007

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2008

Completed
1.4 years until next milestone

Results Posted

Study results publicly available

February 19, 2010

Completed
Last Updated

February 19, 2010

Status Verified

October 1, 2008

Enrollment Period

1.7 years

First QC Date

February 27, 2007

Results QC Date

April 8, 2009

Last Update Submit

January 29, 2010

Conditions

Keywords

PioglitazoneHepatic SteatosisLiver ToxicityLiver BiopsyHIVTreatment ExperiencedTreatment Naive

Outcome Measures

Primary Outcomes (1)

  • Hepatic Steatosis

    Evaluation of the safety and potential benefits of pioglitazone therapy on hepatic steatosis in HIV-infected men and women.

    96 weeks

Secondary Outcomes (1)

  • Insulin Resistance

    48 weeks

Interventions

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Men and women, 18 years of age or greater.
  • Confirmed HIV infection by ELISA and Western blot.
  • No changes in antiretroviral regimen within the prior 3 months. Individuals not currently taking antiretroviral therapy will be eligible.
  • Liver-to-spleen attenuation ratio less than 1 determined by CT and hepatic steatosis on liver biopsy within the past 1 year scored grade 1 or greater (i.e. greater than or equal to 5 percent of hepatocytes).
  • Fasting glucose less than 126 mg/dL.
  • Platelets greater than 50,000/microliters.
  • Willingness to avoid medications and herbal supplements that may increase the risk of bleeding for one week prior to and one week following liver biopsy (e.g. aspirin, NSAIDs and ginko biloba).
  • Willingness to restrict physical activity 72 hours after liver biopsy.
  • Willingness to use 2 effective forms of contraception during the study to avoid pregnancy.
  • Have a primary care physician.

You may not qualify if:

  • Current thiazolidinedione use or use in the last 6 months; known allergy or sensitivity to a thiazolidinedione.
  • Use of insulin or other oral hypoglycemics, or known diabetes.
  • Current pregnancy, breast feeding, or pregnancy within the past 6 months.
  • MELD score greater than 9 or previously diagnosed cirrhosis.
  • ALT greater than 3 times the upper limit of normal.
  • Current or history of heart failure (NYHA Class III or IV cardiac status).
  • Hemoglobin level less than 9g/dL.
  • Active or ongoing infection with Hepatitis A, B, or C.
  • Known or suspected liver disease such as autoimmune hepatitis, Wilson's disease, alpha-1-antitrypsin deficiency, cystic fibrosis, hemachromatosis, glycogen storage disease, amyloidosis, primary biliary cirrhosis, sclerosing cholangitis or any primary or secondary hepatic tumor.
  • Current alcohol/substance abuse or mean alcohol consumption greater than 24g/day over past year.
  • Use of growth hormone, prednisone or other anabolic agents (except for physiologic testosterone replacement) currently or within the past 6 months. One day or less of corticosteroid within the prior 90 days of screening is allowed as is stable dose inhalation corticosteroids.
  • Concurrent use of ketoconazole.
  • Active opportunistic infection (except thrush) or neoplasm (except Kaposi's sarcoma, skin cancer, cancer of the cervix or anus).
  • Any known contraindications to percutaneous liver biopsy including elevated PT/PTT.
  • Severe psychiatric illness that would interfere with adherence to protocol requirements.
  • +3 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, Maryland, 20892, United States

Location

Related Publications (3)

  • Jain MK, Skiest DJ, Cloud JW, Jain CL, Burns D, Berggren RE. Changes in mortality related to human immunodeficiency virus infection: comparative analysis of inpatient deaths in 1995 and in 1999-2000. Clin Infect Dis. 2003 Apr 15;36(8):1030-8. doi: 10.1086/368186. Epub 2003 Apr 2.

    PMID: 12684916BACKGROUND
  • Carr A, Samaras K, Chisholm DJ, Cooper DA. Pathogenesis of HIV-1-protease inhibitor-associated peripheral lipodystrophy, hyperlipidaemia, and insulin resistance. Lancet. 1998 Jun 20;351(9119):1881-3. doi: 10.1016/S0140-6736(98)03391-1.

    PMID: 9652687BACKGROUND
  • Carr A, Miller J, Law M, Cooper DA. A syndrome of lipoatrophy, lactic acidaemia and liver dysfunction associated with HIV nucleoside analogue therapy: contribution to protease inhibitor-related lipodystrophy syndrome. AIDS. 2000 Feb 18;14(3):F25-32. doi: 10.1097/00002030-200002180-00001.

    PMID: 10716495BACKGROUND

MeSH Terms

Conditions

HIV InfectionsFatty LiverInsulin Resistance

Interventions

Pioglitazone

Condition Hierarchy (Ancestors)

Blood-Borne InfectionsCommunicable DiseasesInfectionsSexually Transmitted Diseases, ViralSexually Transmitted DiseasesLentivirus InfectionsRetroviridae InfectionsRNA Virus InfectionsVirus DiseasesGenital DiseasesUrogenital DiseasesImmunologic Deficiency SyndromesImmune System DiseasesLiver DiseasesDigestive System DiseasesHyperinsulinismGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic Diseases

Intervention Hierarchy (Ancestors)

ThiazolidinedionesThiazolesSulfur CompoundsOrganic ChemicalsAzolesHeterocyclic Compounds, 1-RingHeterocyclic Compounds

Limitations and Caveats

Early termination prior to enrollment leading to no analysis of enrolled participants receiving Pioglitazone or placebo.

Results Point of Contact

Title
Colleen Hadigan, MD, MPH
Organization
National Institute of Allergy and Infectious Diseases

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
NIH

Study Record Dates

First Submitted

February 27, 2007

First Posted

February 28, 2007

Study Start

February 1, 2007

Primary Completion

October 1, 2008

Last Updated

February 19, 2010

Results First Posted

February 19, 2010

Record last verified: 2008-10

Locations