Pharmacokinetic Interactions Between DMPA and LPV/r Among HIV-Infected Women
Public ClinicalTrials.gov record NCT01296152. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
An Open-Label, Non-Randomized Study of Pharmacokinetic Interactions Between Depo-Medroxyprogesterone Acetate (DMPA) and Lopinavir/Ritonavir (LPV/r) and of the Effects of DMPA on Cellular Immunity and Regulation in HIV-Infected Women
Study identification
- NCT ID
- NCT01296152
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2
- Lead sponsor
- Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
- Network
- Enrollment
- 25 participants
Conditions and interventions
Conditions
Interventions
- depo-medroxyprogesterone acetate Drug
Drug
Eligibility (public fields only)
- Age range
- 13 Years and older
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Apr 30, 2011
- Primary completion
- Sep 30, 2012
- Completion
- Sep 30, 2012
- Last update posted
- Dec 21, 2015
2011 – 2012
United States locations
- U.S. sites
- 13
- U.S. states
- 9
- U.S. cities
- 10
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Southern California LA (5048) | Los Angeles | California | 90033 | — |
| Children's National Medical Center Washington DC NICHD CRS (5015) | Washington D.C. | District of Columbia | 20010 | — |
| Washington Hospital Center NICHD CRS (5023) | Washington D.C. | District of Columbia | 20010 | — |
| South Florida Childrens Diagnostic & Treatment Cen (5055) | Fort Lauderdale | Florida | 33316 | — |
| Northwestern University CRS (2701) | Chicago | Illinois | 60611 | — |
| Rush University Cook County Hospital Chicago NICHD CRS (5083) | Chicago | Illinois | 60612 | — |
| Tulane University New Orleans NICHD CRS (5095) | New Orleans | Louisiana | 70112 | — |
| Univ. of Rochester ACTG CRS (1101) | Rochester | New York | 14642 | — |
| SUNY Stony Brook NICHD CRS (5040) | Stony Brook | New York | 11794 | — |
| Unc Aids Crs (3201) | Chapel Hill | North Carolina | 27516 | — |
| Univ. of Cincinnati CRS | Cincinnati | Ohio | 45267-0405 | — |
| Univ. of Cincinnati CRS (2401) | Cincinnati | Ohio | 45267 | — |
| University of Washington AIDS CRS (1401) | Seattle | Washington | 98104 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01296152, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Dec 21, 2015 · Synced Jul 24, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01296152 live on ClinicalTrials.gov.