Treatment Approaches for Preeclampsia in Low-Resource Settings
Preeclampsia
About this trial
This is an interventional treatment trial for Preeclampsia focused on measuring Preeclampsia, Eclampsia, Magnesium Sulfate
Eligibility Criteria
Inclusion Criteria:
- Exhibit systolic blood pressure > 140mm Hg OR a diastolic pressure > 100 mm Hg;
- Exhibit proteinuria > 1+;
- Have not given birth, or be 24h or less postpartum;
- Exhibit urine output >100 ml or more during the previous 4h or greater than 25 mL/h;
- Agree to comply with study procedures;
- Be > 18 years of age;
- Give informed consent for study participation
Exclusion Criteria:
- Eclamptic or seizing at the time of enrollment
- Received magnesium sulfate therapy 24h prior to study enrollment
Sites / Locations
- Government Medical College
- Christian Medical College
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
2
1
Women in Group II (standard of care) will receive an 8 mL loading dose containing 4g magnesium sulfate administered manually per standard hospital protocol. The solution will be diluted with normal saline according to standard hospital practice, and given IV over 20 minutes. For women in Group II, the IV loading dose will be followed immediately with 20 mL treatment by IM injection, given as 10 mL (5 g magnesium sulfate) into each buttock. This dose will be followed by 10 mL treatments (5g magnesium sulfate) every four hours, injected into alternate buttock. Treatment will be discontinued when clinically indicated.
Women in Group I (Springfusor® arm) will receive a 8 mL loading dose containing 4g magnesium sulfate heptahydrate (MgSO4*7H2O) 50% solution, which is approximately 2 mmoL magnesium/mL. The loading dose of 8mL with 4 g MgSO4will be administered using the Springfusor® pump. For women in Group I, the administration of the loading dose will be immediately followed by a maintenance infusion. The maintenance dose of 4 g (8 cc, 50% MgSO4) will be administered with the Springfusor® pump continuously over four hours. The pump will be started immediately after the initial bolus and the 4g dose repeated (and syringe replaced) every four hours for upto 24 hours postpartum.