A Study to Collect Information About HIV-Positive Pregnant Women and Their Babies
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|ClinicalTrials.gov Identifier: NCT00000910|
Recruitment Status : Completed
First Posted : August 31, 2001
Last Update Posted : October 7, 2013
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.
|Condition or disease|
|HIV Infections Pregnancy|
The population served at affiliated ACTG sites has not been officially described. Anecdotal evidence, however, has surfaced regarding the characteristics of HIV-infected pregnant women and the current standard of care during pregnancy. This chart abstraction study is designed to define, more accurately, the pertinent characteristics and general numbers of women in these trials.
In this medical chart abstraction study, pertinent information is collected on all HIV-infected pregnant women and their infants who receive primary or consultative care at PACTG 367 study sites. Part A profiles all HIV-infected women who received care or consultation at study sites and who had a pregnancy outcome between January 1, 1998 through July 1, 1998. [AS PER AMENDMENT 04/12/02: Part A is closed to enrollment.] Part B profiles HIV-infected pregnant women who receive primary or consultative care and a pregnancy outcome following July 1, 1998.
|Study Type :||Observational|
|Enrollment :||2000 participants|
|Official Title:||Medical Chart Abstraction of HIV-Infected Pregnant Women and Their Infants Receiving Care or Consultation at Study Sites|
|Actual Study Completion Date :||June 2004|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00000910
|United States, Massachusetts|
|Brigham and Women's Hosp., Div. of Infectious Disease|
|Boston, Massachusetts, United States, 02115|
|United States, New Jersey|
|Rutgers - New Jersey Medical School CRS|
|Newark, New Jersey, United States, 07103|
|Study Chair:||Ruth Tuomala|
|Study Chair:||Renee Samelson|