Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
616 participants
OBSERVATIONAL
2016-03-31
2017-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Swaziland Safe Generations
NCT01891799
Option B+: Study on Safety, Viral Suppression, and Survival on Second Line ART
NCT02249962
Evaluation of the Population-level Impact of PMTCT Option B+ in Zimbabwe
NCT03388398
Postpartum Adherence Clubs to Enhance Support: the PACER Study
NCT02417675
Long Term Outcomes of Therapy in Women Initiated on Lifelong ART Because of Pregnancy in DR Congo
NCT03048669
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Determined to be LTF per the Safe Generations study protocol (i.e., have not attended a clinic visit in the 90 days prior to their 6-month postpartum appointment and are not known to be dead or transferred out, according to clinical visit data abstracted to the Safe Generations study database).
Exclusion Criteria
1 Year
50 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ministry of Health, Swaziland
OTHER_GOV
Columbia University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
William Reidy
Associate Research Scientist, ICAP
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
William Reidy, PhD
Role: PRINCIPAL_INVESTIGATOR
ICAP at Columbia University
Elaine Abrams, PhD
Role: STUDY_DIRECTOR
ICAP at Columbia University
Averie Gachuhi, MSc
Role: STUDY_DIRECTOR
ICAP at Columbia University
Harriet Nuwagaba-Biribonwoha, MBChB, PhD
Role: STUDY_DIRECTOR
ICAP at Columbia University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Family Life Association Swaziland (FLAS) Manzini
Swaziland, , Eswatini
King Sobhuza II Hospital
Swaziland, , Eswatini
Luyengo Clinic
Swaziland, , Eswatini
Mankayane PHU
Swaziland, , Eswatini
Mbikwakhe Clinic
Swaziland, , Eswatini
Médecins sans Frontières (MSF) Matsapha
Swaziland, , Eswatini
Raleigh Fitkin Memorial Hospital
Swaziland, , Eswatini
Siphofaneni Clinc
Swaziland, , Eswatini
Siteki PHU
Swaziland, , Eswatini
Lamvelase
Zombodze, , Eswatini
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AAAP5700
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.