A Cohort Study for Occupational Stress Induced Early Embryonic Death
NCT ID: NCT02115438
Last Updated: 2014-04-16
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
3405 participants
OBSERVATIONAL
2010-03-31
2013-01-31
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.
Fetal Brain Growth - Pilot Study
NCT05994443
Prediction of Spontaneous Preterm Birth by Cervical Elastogram
NCT03601195
A New Birth Weight Prediction in Chinese Population
NCT03223363
Interrelations Between Spontaneous Otoacoustic Emissions and Transient Evoked Emissions
NCT01325272
Maternal Voice and Quantitative EEG (qEEG)
NCT05391633
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
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Occupational Stress
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. the gestational age is less than 14 weeks;
3. pregnant women and their spouses have jobs before treatment.
Exclusion Criteria
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Peking University Third Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yiming Zhao
Director of Research Center of Clinical Epidemiology
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
54416-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.