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 @ 11:46 PM
Ignite Modification Date:
2025-12-24 @ 11:46 PM
NCT ID:
NCT02813551
Eligibility Criteria:
Inclusion Criteria:
* Postpartum women at ≥ 18 years of age
* Antepartum/intrapartum or within 24 hours postpartum diagnosis of either:
* Preeclampsia
* Preeclampsia with severe features
* Preeclampsia superimposed to chronic hypertension
Exclusion Criteria:
* Chronic hypertension without superimposed preeclampsia
* Gestational hypertension
* Urine output \< 30 cc/h at time of randomization
* Heart failure or pulmonary edema
* Hypersensitivity to Torsemide or sulfonylureas
* Hypokalemia (serum potassium \< 3 mEq/L)
* Preexisting diuretic use within 24 hours prior to randomization
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT02813551
Study Brief:
Protocol Section:
NCT02813551