A Study to Collect Information About HIV-Positive Pregnant Women and Their Babies
Medical Chart Abstraction of HIV-Infected Pregnant Women and Their Infants Receiving Care or Consultation at Study Sites
3 other identifiers
observational
2,000
1 country
2
Brief Summary
The purpose of this study is to collect medical information about HIV-positive pregnant women and their babies who have been (or are being) seen at study sites. This information will be used to help design future research studies for these patients. The population of HIV-positive pregnant women and their babies who are seen at study sites has not been officially examined. In order to design future studies to research the best care for these patients, this study will examine important characteristics and the general number of women in these trials.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
2 active sites
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
First Submitted
Initial submission to the registry
November 2, 1999
CompletedFirst Posted
Study publicly available on registry
August 31, 2001
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2004
CompletedOctober 7, 2013
October 1, 2013
November 2, 1999
October 4, 2013
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- A patient may be eligible for this study if she:
- Is an HIV-positive woman.
- Is receiving care at a study site during the study period or her infant is receiving care at a study site and whose delivery information is available.
- Had a baby on or after January 1, 1998.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Brigham and Women's Hosp., Div. of Infectious Disease
Boston, Massachusetts, 02115, United States
Rutgers - New Jersey Medical School CRS
Newark, New Jersey, 07103, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Ruth Tuomala
- STUDY CHAIR
Renee Samelson
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 2, 1999
First Posted
August 31, 2001
Study Completion
June 1, 2004
Last Updated
October 7, 2013
Record last verified: 2013-10