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 @ 10:36 PM
Ignite Modification Date:
2025-12-24 @ 10:36 PM
NCT ID:
NCT02059135
Eligibility Criteria:
Inclusion Criteria:
1. Hospitalized female pregnant patients of gestational age of ≥23 0/7 weeks to ≤30 0/7 weeks (for subjects at gestational age 23 0/7 to 23 6/7 all standard interventions including antenatal steroids and cesarean for fetal indications must be offered).
Gestational age determination by local practice using one of the following three approaches:
* Last menstrual period (LMP) dating and confirmatory ultrasound
* Ultrasound alone when LMP is not reliable
* Known date of conception in the setting of assisted reproductive technology
2. At least 16 years of age (NOTE: different age restrictions may apply per local regulation and/or ethical considerations; subjects under the local age of consent may be excluded at the discretion of the reviewing Institutional Review Board (IRB)
3. Recent diagnosis of Preeclampsia or Superimposed Preeclampsia as defined by:
• For Preeclampsia
* Gestational hypertension defined as a recorded systolic blood pressure (BP) of
≥140 mm Hg or diastolic BP of ≥90 mm Hg on 2 occasions at least 4 hours apart (since the commencement of medical intervention in any facility) OR
* Severe gestational hypertension defined as systolic blood pressure of ≥ 160 mm Hg or diastolic blood pressure ≥ 110 mm Hg, confirmed with second assessment within a short interval (minutes) AND
* New onset of any of the following:
* Proteinuria defined as ≥0.3 g protein per 24 hours in a 12-24 hour urine collection or protein/creatinine ratio of ≥0.3 mg/mg\* (on a random sample or any collection period.)
* Platelet count less than 100,000/μL
* Serum creatinine concentrations greater than 1.1 mg/dL in the absence of other renal disease
* Elevated liver transaminases to ≥ twice upper limit of normal
* Cerebral or visual symptoms
For Superimposed preeclampsia:
* The start of antihypertensive medication, increasing the dose of a currently administered antihypertensive medication or adding a second antihypertensive medication after 20 weeks of pregnancy for systolic BP ≥ 160 or diastolic BP ≥ 105 in a patient that had a previous history of controlled hypertension before 20 weeks of pregnancy. AND
* New onset of any of the following:
* proteinuria defined as ≥0.3 g protein per 24 hours in a 12-24 hour urine collection or protein/creatinine ratio of ≥0.3 mg/mg (on a random sample or any collection period)
* Platelet count less than 100,000/μL
* Serum creatinine concentrations greater than 1.1 mg/dL in the absence of other renal disease
* Elevated liver transaminases to ≥ twice upper limit of normal
* Cerebral or visual symptoms
4. In the opinion of the investigator the patient has demonstrated sufficient clinical stability to be eligible for expectant management
5. The patient is expected to be managed as an inpatient until delivery
6. Signed informed consent for both subject and neonate
Exclusion Criteria:
1. Criteria that would likely require immediate delivery of the fetus are exclusionary if present just prior to randomization:
* Refractory hypertension despite maximal medical intervention of systolic BP ≥160 mm Hg or diastolic BP of ≥110 mm Hg
* Thrombocytopenia (platelets ˂ 100/mm3) with or without Hemolysis elevated liver enzymes low platelets (HELLP) syndrome defined as defined as Aspartate amino transferase (AST) ≥70 units/L, and platelets ˂100/mm3, and evidence of hemolysis on blood film plus either Lactic dehydrogenase (LDH) ≥600 IU/mL or total bilirubin ≥1.2 mg/dL)
* Oliguria (≤500 mL/24 hours) or evidence of progressive renal insufficiency
* Serum creatinine concentration greater than 1.1 mg/dL
* Persistent visual disturbances
* Placental abruption
* Pulmonary edema
* Nonreassuring fetal heart rate tracing
* Intractable headache unrelieved with analgesia
* Intractable right upper quadrant abdominal pain or vomiting
* If umbilical Doppler ultrasound has been performed, the presence of an abnormal umbilical artery Doppler as defined by absent or reverse end diastolic flow
* Biophysical score ≤ 4/10 on 2 occasions
* Oligohydramnios (deepest vertical pocket less than 2 x 2cm on ultrasound)
* Other maternal or fetal conditions that would preclude expectant management
2. Known lethal or major fetal anomaly
3. Recent (within 12 months) history of maternal alcoholism or drug dependence
4. Diagnosis of epilepsy
5. Has need for chronic therapy with nonsteroidal anti-inflammatory drugs (NSAIDs) including selective cyclooxygenase (Cox)-2 inhibitors, or unwilling to abstain from use of NSAIDs during the study treatment period (low dose aspirin of 81 mg/day or less allowable)
6. Received within 72 hours or has requirement for heparin; low molecular weight heparins such as enoxaparin or dalteparin; fondaparinux; antiplatelet agents such as clopidogrel, prasugrel, or high dose aspirin (\>81 mg/day); Direct Thrombin Inhibitors (DTI) such as dabigatran
7. Pre-existing renal disease, documented pre-pregnancy or in pregnancy prior to 20 weeks gestation (prior to the diagnosis of preeclampsia) or 24 hr urine of ≥0.3 gm/24 hours, documented in pregnancy, prior to 20 weeks gestation or ≥2+ dipstick or ≥ 0.3 Protein Creatinine Ratio (PCR), documented in pregnancy at the last available test prior to 20 weeks gestation. In the case of conflicting results between dipstick, PCR, and timed urine collection tests to work up an episode of proteinuria, the timed urine collection result would supersede other results
8. Multi-fetal pregnancy
9. History of Antiphospholipid antibody syndrome
10. Known hypersensitivity to goat and goat milk proteins
11. Participation in another interventional clinical trial of an investigational, unapproved therapy (drug, biologic, device) within 30 days of consent
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
16 Years
Study:
NCT02059135
Study Brief:
Protocol Section:
NCT02059135