Efficacy of Diltiazem for the Control of Blood Pressure in Puerperal Patients With Severe Preeclampsia
Postpartum Preeclampsia
About this trial
This is an interventional treatment trial for Postpartum Preeclampsia
Eligibility Criteria
Inclusion Criteria:
The following parameters of all patients were within the normal range: hematic biometry, urine and glucose tests, aspartate aminotransferase (AST), alanine aminotransferase (ALT), serum creatinine, blood coagulation test including prothrombin time and activated partial thromboplastin time. Electrocardiogram and chest radiography showed no pathological data.
Exclusion Criteria:
When the patient falls outside of the aforementioned parameters, or subjects with unstable medical conditions.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Diltiazem
Nifedipine
Postpartum patients were administered (60 mg) orally every 8 hours with diltiazem (tables).
Postpartum patients were administered (10 mg) orally every 8 hours with nifedipine (capsule).