Risk of Cesarean Section in Primiparous Women Over 35 Years of Age.
NCT ID: NCT03771976
Last Updated: 2018-12-13
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
572 participants
OBSERVATIONAL
2017-04-01
2018-02-23
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Over 35 years of age
Primiparous women over 35 years of age.
Cesarean section
Risk of cesarean section between the cohorts
No cesarean section
Vaginal birth rate between the cohorts
Between 20-34 years of age
Primiparous women between 20 and 34 years of age.
Cesarean section
Risk of cesarean section between the cohorts
No cesarean section
Vaginal birth rate between the cohorts
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Cesarean section
Risk of cesarean section between the cohorts
No cesarean section
Vaginal birth rate between the cohorts
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Birth after 22 weeks and neonatal weight \> 501g.
Exclusion Criteria
* Birth before 22 weeks or neonatal weight \< 500g.
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Saint Thomas Hospital, Panama
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Osvaldo A. Reyes T.
Chairman of Research - Saint Thomas Maternity Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Saint Thomas H
Panama City, , Panama
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.
MHST-2014-05
Identifier Type: -
Identifier Source: org_study_id