Clinical Trial Search

Primary: Number of Subjects Who Achieved 'Success' Meaning a ≥ 2.0 Increase in Hemoglobin — 162; 159 participants

Primary: Hemoglobin Level — 12; 12 grams/deciliters

Primary: Total Number of Units Transfused — 1.2; 2.1 units of blood — p=<0.001

Primary: Maternal Anemia at Delivery — 4; 11 Participants — p=0.039

Primary: Difference in Actual Blood Volume and Estimated Blood Volume in Milliliters. — -20.8; -41.7; -53.5; -96.0 milliliters — p=<0.05

Primary: Number of Patients Classified as a 'Clinical Success'. Clinical Success Was Defined as the Number of Subjects With an Increase in Hemoglobin of >12 g/dL — 127; 98…

Primary: Evaluate the Safety of the Maximum Administered Dose, 15 mg/kg (up to a Maximum 1,000 mg) of FCM Compared to SMC. — 6; 22 participants

Primary: Percent of Non-anemic Patients With Iron Deficiency Stratified by Gravidity — 9; 3; 6; 38 Participants

Primary: Fibrinogen Level at 2 Hours After Delivery — 186; 418 mg/dL — p=<0.05

Primary: Recruitment Feasibility — 10 percentage eligible and enrolled

Primary: PK Model Parameter Estimates — 8.85; 10.39; 9.45 L/hr

Primary: Change From Baseline Resilience at 4 Weeks — 26.57; 28.29; 1.85 score on a scale — p=<.001

Primary: Median Change in Hemoglobin Value Before and After Intervention — 10.95; 11.45 g/dL — p=< 0.001

Primary: Hematocrit (Hct) — 29.2; 28.3 percentage of red blood cells in blood

Primary: The Incidence of Early Onset Sepsis in VLBW Infants With AOP. — 18; 34; 7; 42 Participants

Primary: Number of Transfusions During Hospitalization — 1.2; 1.2; 2.4 number of transfusions

Primary: Quantitative Blood Loss — 840; 1051 milliliters — p=<0.05

Primary: Blood-oxygen-level-dependent (BOLD) Response During Functional Magnetic Resonance Imaging (fMRI) z Statistic — 2.3; 2.0; 2.1; 1.7 z score — p=.27

Primary: Percentage of Women Who Achieve Anemia Correction After a Single Dose of 1000mg of Low Molecular Weight Iron Dextran(INfeD). — 35; 11 Participants

Primary: Change in Edinburgh Depression Scale From Baseline — 17.81; 17.9; 12.04; 11.41 units on a scale

Primary: NT-proBNP Levels at 4-6 Weeks Postpartum — 36.5; 39.5 pg/mL — p=0.49

Primary: The Primary Outcome is Iron Depletion, and Will be Defined as Serum Ferritin <10 mcg/L. — 64; 71; 13; 10 participants — p=0.42

Primary: Haemoglobin Level — 88.3; 89.2; 88.4; 89.6 g/L — p=<0.05

Primary: Patient Indication of Willingness to Accept the Vaccine Based on Survey — 56 Participants

Primary: Proportion of Participants With Recorded Blood Pressure Values in Office — 43; 44; 49; 56 Participants

Primary: Duration of Breastfeeding Among Women Who Plan to Breastfeed Their Infants After Postpartum or Delayed (4-6 Weeks Postpartum) Initiation of DMPA — 71; 70; 4; 4…

Primary: Feasibility of Enrolling Patients in the Trial — 85 participants

Primary: Score on the Edinburgh Postnatal Depression Scale (EPDS) — 5.04; 4.36; 4.43; 4.04 score on a scale

Primary: The Primary Outcome is a Composite of the Following Three Clinical Outcomes: 1) Severe PPH Defined as Blood Loss ≥1000 ml or; 2) Postpartum Laparotomy for Bleeding or…

Primary: Depression Symptoms — 10.1; 11 score on a scale