Expired Study
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Rockville, Maryland 20852


Purpose:

The purpose of this study is to find out if the anti-HIV drugs nelfinavir (NFV), lopinavir/ritonavir (LPV/r), and efavirenz (EFV) change the amount of estrogen in the blood when taken along with hormone replacement therapy (HRT) for menopause. HRT can be helpful for treating bothersome symptoms of menopause. However, it is not routinely used in HIV-infected postmenopausal women because it is not known how HRT interacts with anti-HIV drugs. The information obtained from this study will help doctors make recommendations for HRT in postmenopausal HIV-infected women.


Study summary:

The benefits of hormone replacement therapy (HRT) in HIV-negative postmenopausal women include the abatement of menopausal symptoms such as hot flashes, insomnia, mood changes, vaginal dryness, urogenital and skin changes, and memory loss. HRT may also decrease risk for primary cardiovascular disease, osteoporosis, colon cancer, and possibly Alzheimer's disease and age-related macular degeneration. There may also be an overall survival benefit for HIV-negative postmenopausal women taking hormone replacement therapy. Despite the potential benefits of postmenopausal hormone replacement, it is seldom used in HIV-infected postmenopausal women. One concern about HRT in HIV-infected women is the potential for interaction with antiretroviral (ARV) drugs. Although the effect of HRT on ARV drug levels is likely to be small, it is important to evaluate the safety of administering HRT concurrently with ARVs. The information obtained from this study will help shape recommendations for postmenopausal HRT in HIV-infected women. Patients are enrolled into 1 of 4 study arms based on their current oral ARV regimens. Arm A takes NFV plus nucleoside reverse transcriptase inhibitors (NRTIs). Arm B takes LPV/r plus NRTIs. Arm C takes EFV plus NRTIs. Arm D enrolls HIV-infected patients not on current ARVs, or who are taking NRTIs only (no protease inhibitors [PIs] or nonnucleoside reverse transcriptase inhibitors [NNRTIs]). All arms receive HRT with oral estradiol and medroxyprogesterone acetate for 12 weeks. Arms A, B, and C have intensive PI or NNRTI pharmacokinetic (PK) sampling at entry and Week 4. All arms have estradiol PK sampling at Week 4. Clinical and laboratory evaluations are done at entry, Week 4, and Week 12. ARVs are not provided by this study. Only HRT is provided.


Criteria:

Inclusion Criteria Patients may be eligible for this study if they: - Are postmenopausal women over 18 years old. - Are infected with HIV. - Have a CD4 cell count of 100 cells/mm3 or greater within 45 days prior to study entry. - Have a plasma viral load less than 55,000 copies/ml within 45 days prior to study entry. - Are willing to comply with study requirements. These include not changing smoking habits during the course of the study and not consuming caffeine or alcohol prior to PK sampling. - Have had a Pap smear within 12 months prior to study entry. - Meet one of the following requirements: a) patients must currently be on stable PI or EFV regimens plus 2 or more acceptable NRTIs, or b) patients must not currently be taking any ARVs, with the exception of an NRTI-only regimen. - Have a way to obtain their ARVs outside of the study and agree to continue their ARV regimen for at least 12 weeks of the study. Exclusion Criteria Patients may not be eligible for this study if they: - Have had breast or endometrial cancer, thrombophlebitis, or thromboembolism. - Have had serious nausea, vomiting, or abdominal pain within 30 days prior to study entry. - Have had a serious illness requiring systemic treatment and/or hospitalization within 14 days prior to study entry. - Are allergic or sensitive to the drugs that will be used for HRT. - Have undiagnosed postmenopausal bleeding. - Have coronary artery disease. - Have used hormonal therapies within 8 weeks prior to study entry. - Have used DMPA (Depo Provera) within 180 days prior to study entry. - Have used the anti-HIV drugs ZDV and d4T at the same time within 30 days prior to study entry. - Have used other medications specified in the protocol within 30 days prior to study entry. - Are using experimental drugs without the written approval of the study co-chairs. - Are unable to adhere to the ARV or HRT medications while on study, in the opinion of the investigator.


NCT ID:

NCT00044837


Primary Contact:

Study Chair
Lori Kamemoto


Backup Contact:

N/A


Location Contact:

Rockville, Maryland 20852
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 11, 2017

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