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Different Schemes of Magnesium Sulfate for Preeclampsia (MGSO4)

Primary Purpose

Preeclampsia

Status
Terminated
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Magnesium sulfate 50% - 1g/h
Magnesium sulfate 50% - 2g/h
Sponsored by
Instituto Materno Infantil Prof. Fernando Figueira
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preeclampsia

Eligibility Criteria

14 Years - 50 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Severe Preeclampsia (pure and superimposed)

Exclusion Criteria:

  • Eclampsia before administration of the loading dose of MgSO4 ;
  • Use of other medications or illicit drugs that may interfere with maternal hemodynamics;
  • Contraindications to the use of magnesium sulfate: known hypersensitivity to the drug, oliguria with urine output below 25 ml per hour or anuria (urine output absent) and myasthenia gravis.
  • Use of mechanical ventilation

Sites / Locations

  • Instituto Materno Infantil Prof. Fernando Figueira

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Magnesium sulfate 50% - 1g/h

Magnesium sulfate 50% - 2g/h

Arm Description

After loading dose of 6g of magnesium sulfate, patients will receive the maintenance dose of 1g/hour of intravenous magnesium sulfate, for 24 hours

After loading dose of 6g of magnesium sulfate, patients will receive the maintenance dose of 2g/hour of intravenous magnesium sulfate, for 24 hours

Outcomes

Primary Outcome Measures

ECLAMPSIA
Seizures that occur after the loading dose, during magnesium sulfate, until 24 hours after the delivery of the baby

Secondary Outcome Measures

Placental abruption
Occurence of placental abruption
postpartum hemorrhage
Occurence of postpartum hemorrhage, diagnosed clinically by the attending phisician
COMPLICATIONS
Occurence of a retained placenta
thromboembolic complications
Diagnosis of thromboembolic complications bay doppler compression ultrasound or CT
liver failure
Occurence of liver failure according to laboratorial exams
OLIGURIA
Oliguria diagnosed as the presence of urine output under 0.5 (mililiters per kilogram) mL/kg for six hours,
RENAL FAILURE
Occurence of renal failure diagnosed as the presence of oliguria for more than 24 hours or elevation serum creatinine (3X )
Disseminated intravascular coagulation (DIC)
Presence of disseminated intravascular coagulation
acute pulmonary edema
Presence of clinically diagnosis of acute pulmonary edema
Maternal death
Maternal death occuring for direct obstetric causes
Composite maternal morbidity
Presence of one of the investigated complications
RECURRENCE
Recurrence of seizures after loading dose of magnesium sulfate
additional anticonvulsant
Need for additional anticonvulsant after the use of magnesium sulfate
SIDE EFFECTS
Presence of side effects of magnesium sulfate use
DISCONTINUATION OF MAGNESIUM SULFATE
Occurence of discontinuation of treatment due to side effects
GLUCONATE USE
Need for the use of calcium gluconate
MAGNESIUM LEVELS
Serum magnesium levels evaluated at the beginning of maintenance dose and after 30. minutes, every 2 hours for six hours and after every six hours until 24 hous after loading dose. This outcome will be evaluated in the first 62 patients
Hypertensive crises
Presence of hypertensive crises and need for antihypertensive drugs and need to continue therapy for more than 24 hours.

Full Information

First Posted
March 10, 2015
Last Updated
December 19, 2016
Sponsor
Instituto Materno Infantil Prof. Fernando Figueira
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1. Study Identification

Unique Protocol Identification Number
NCT02396030
Brief Title
Different Schemes of Magnesium Sulfate for Preeclampsia
Acronym
MGSO4
Official Title
Effectiveness and Safety of 1g/Hour vs. 2g/Hour of Magnesium Sulfate Maintenance Dose for Eclampsia Prevention: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Terminated
Why Stopped
After recommendation because of the impossibility to end study with 1 center only. Outcomes of patients already included will be evaluated.
Study Start Date
March 2015 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Materno Infantil Prof. Fernando Figueira

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Eclampsia is an obstetric emergency capable of prophylaxis. To prevent and control seizures, there is no doubt that the magnesium sulfate (MgSO4) is the ideal drug. However, there are still questions regarding its use and dose. The scheme and the optimal time of administration remain to be elucidated. The objective of this trial is to compare the effectiveness and safety of intravenous magnesium sulfate in the maintenance phase 1g / h versus 2 g / h to prevent eclampsia in pregnant and postpartum women with severe preeclampsia (pure or superimposed).
Detailed Description
Hypertensive disorders are frequent during the course of pregnancy-puerperal cycle and an important cause of maternal morbidity and mortality, fetal and perinatal. The high frequency of maternal death can be explained by the presence of numerous complications such as eclampsia. Eclampsia is an obstetric emergency capable of prophylaxis. To prevent and control seizures, there is no doubt that the magnesium sulfate (MgSO4) is the ideal drug. However, there are still questions regarding its use and dose. The scheme and the optimal time of administration remain to be elucidated. Currently, allows the use of either 1 g / h to 2 g / h of magnesium sulphate during the maintenance phase to prevent eclamptic convulsions. However, there is no report in the literature of randomized controlled trials comparing different doses of magnesium sulfate in the maintenance phase to prevent eclampsia. The objective of this study is to compare the effectiveness and safety of intravenous magnesium sulfate in the maintenance phase 1g / h versus 2 g / h to prevent eclampsia in pregnant and postpartum women with severe preeclampsia (pure or superimposed).There will be a trial randomized and triple blind in the Integrative Medicine Institute Prof. Fernando Figueira (IMIP) from March 2015 to April 2017, and will be included 2000 women randomized into two groups: MgSO4 maintenance dose of 1 g / h or 2 g / h. Patients who had eclampsia before loading dose, with use of other medications or illicit drugs that may interfere with maternal hemodynamics or with contraindications to the use of magnesium sulfate will be excluded. The primary endpoint will be the incidence of eclampsia. Other complications such as oliguria, bleeding, recurrence of seizures, disseminated intravascular coagulation, maternal death, presence of side effects related to the use of MgSO, neonatal outcome and other variables will be considered secondary outcomes. Randomization for preventive treatment of eclamptic seizures with MgSO4 1g / h or MgSO4 2g / h will be held according to a table of sequential numbers from one to 2000, using the letters A and B and not knowing its meaning. The analysis will be performed with the groups identified as A or B, breaking the secrecy only after the results obtained and prepared the tables, or by resolution of the External Monitoring Committee.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preeclampsia

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Magnesium sulfate 50% - 1g/h
Arm Type
Active Comparator
Arm Description
After loading dose of 6g of magnesium sulfate, patients will receive the maintenance dose of 1g/hour of intravenous magnesium sulfate, for 24 hours
Arm Title
Magnesium sulfate 50% - 2g/h
Arm Type
Experimental
Arm Description
After loading dose of 6g of magnesium sulfate, patients will receive the maintenance dose of 2g/hour of intravenous magnesium sulfate, for 24 hours
Intervention Type
Drug
Intervention Name(s)
Magnesium sulfate 50% - 1g/h
Other Intervention Name(s)
Mg SO4
Intervention Description
Patients will receive after the loading dose os magnesium sulfate, the maintenance dose of 1g/hour of intravenous of magnesium sulfate for 24 hours after loading dose
Intervention Type
Drug
Intervention Name(s)
Magnesium sulfate 50% - 2g/h
Other Intervention Name(s)
MgSO4
Intervention Description
Patients will receive after the loading dose os magnesium sulfate, the maintenance dose of 1g/hour of intravenous of magnesium sulfate for 24 hours after loading dose
Primary Outcome Measure Information:
Title
ECLAMPSIA
Description
Seizures that occur after the loading dose, during magnesium sulfate, until 24 hours after the delivery of the baby
Time Frame
From end of loading dose, until 24 hours after delivery
Secondary Outcome Measure Information:
Title
Placental abruption
Description
Occurence of placental abruption
Time Frame
From end of loading dose, until delivery of the child
Title
postpartum hemorrhage
Description
Occurence of postpartum hemorrhage, diagnosed clinically by the attending phisician
Time Frame
From end of loading dose, until 48 hours after delivery
Title
COMPLICATIONS
Description
Occurence of a retained placenta
Time Frame
From end of loading dose, until 3 hours after delivery
Title
thromboembolic complications
Description
Diagnosis of thromboembolic complications bay doppler compression ultrasound or CT
Time Frame
From end of loading dose, until 15 days after delivery
Title
liver failure
Description
Occurence of liver failure according to laboratorial exams
Time Frame
From end of loading dose, until 15 days after delivery
Title
OLIGURIA
Description
Oliguria diagnosed as the presence of urine output under 0.5 (mililiters per kilogram) mL/kg for six hours,
Time Frame
From end of loading dose, until 15 days after delivery
Title
RENAL FAILURE
Description
Occurence of renal failure diagnosed as the presence of oliguria for more than 24 hours or elevation serum creatinine (3X )
Time Frame
From end of loading dose, until 15 days after delivery
Title
Disseminated intravascular coagulation (DIC)
Description
Presence of disseminated intravascular coagulation
Time Frame
From end of loading dose, until 15 days after delivery
Title
acute pulmonary edema
Description
Presence of clinically diagnosis of acute pulmonary edema
Time Frame
From end of loading dose, until 15 days after delivery
Title
Maternal death
Description
Maternal death occuring for direct obstetric causes
Time Frame
From end of loading dose, until 42 days after delivery
Title
Composite maternal morbidity
Description
Presence of one of the investigated complications
Time Frame
From end of loading dose, until 42 days after delivery
Title
RECURRENCE
Description
Recurrence of seizures after loading dose of magnesium sulfate
Time Frame
From end of loading dose, until 24 hours after delivery
Title
additional anticonvulsant
Description
Need for additional anticonvulsant after the use of magnesium sulfate
Time Frame
From end of loading dose, until 24 hours after delivery
Title
SIDE EFFECTS
Description
Presence of side effects of magnesium sulfate use
Time Frame
From end of loading dose, until 24 hours after delivery
Title
DISCONTINUATION OF MAGNESIUM SULFATE
Description
Occurence of discontinuation of treatment due to side effects
Time Frame
From end of loading dose, until 24 hours after delivery
Title
GLUCONATE USE
Description
Need for the use of calcium gluconate
Time Frame
From end of loading dose, until 24 hours after delivery
Title
MAGNESIUM LEVELS
Description
Serum magnesium levels evaluated at the beginning of maintenance dose and after 30. minutes, every 2 hours for six hours and after every six hours until 24 hous after loading dose. This outcome will be evaluated in the first 62 patients
Time Frame
From end of loading dose, until 24 hours after delivery
Title
Hypertensive crises
Description
Presence of hypertensive crises and need for antihypertensive drugs and need to continue therapy for more than 24 hours.
Time Frame
From end of loading dose, until 24 hours after delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severe Preeclampsia (pure and superimposed) Exclusion Criteria: Eclampsia before administration of the loading dose of MgSO4 ; Use of other medications or illicit drugs that may interfere with maternal hemodynamics; Contraindications to the use of magnesium sulfate: known hypersensitivity to the drug, oliguria with urine output below 25 ml per hour or anuria (urine output absent) and myasthenia gravis. Use of mechanical ventilation
Facility Information:
Facility Name
Instituto Materno Infantil Prof. Fernando Figueira
City
Recife
State/Province
Pernambuco
ZIP/Postal Code
50.070-550
Country
Brazil

12. IPD Sharing Statement

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Different Schemes of Magnesium Sulfate for Preeclampsia

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