Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:16 PM
Ignite Modification Date:
2025-12-24 @ 11:16 PM
NCT ID:
NCT00388856
Eligibility Criteria:
Inclusion Criteria:
* Agree to consent form, and consent to protocol of research
* Known healthy singleton 6-10 weeks pregnant women
Exclusion Criteria:
* Blood pressure \> 135/85
* Proteinuria
* History or current use of anti-hypertensive medication or diuretics
* Use of vitamins C \> 150 mg and/or E \> 75 IU per day
* Pregestational diabetes
* Known placental abnormalities.
* Current pregnancy is a result of in vitro fertilization
* Regular use of platelet active drugs or non-steroidal anti-inflammatory drugs
* Known fetal abnormalities
* Documented uterine bleeding within a week of screening
* Uterine malformations
* History of medical complications
* Illicit drug or alcohol abuse during current pregnancy
* Intent to deliver elsewhere
* Known psychologic problems.
* Participating in another interventional study
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
17 Years
Maximum Age:
45 Years
Study:
NCT00388856
Study Brief:
Protocol Section:
NCT00388856