Child outcomes after prenatal progesterone for prevention of preterm birth, follow-up of the AMPHIA trial
Recruiting
- Conditions
- Prevention of preterm birth in multiple pregnancy
- Registration Number
- NL-OMON27515
- Lead Sponsor
- Amsterdam UMC - location AMC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 300
Inclusion Criteria
The study population consists of all women that participated in the AMPHIA trial (n=671) and their children (n=1355) between 11-14 years of age.
Exclusion Criteria
Not able to read and speak Dutch and therefore not able to give informed consent and fill out questionnaires for this follow-up study.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cognition and behavior of the offspring.
- Secondary Outcome Measures
Name Time Method Death (perinatal and death up to 14 years of age), gender identity and health related problems (including information on surgery, hospital admission and medication use).<br>Educational performance at the end of primary school for all children born to women who participated in the AMPHIA trial (regardless of participation in follow-up).