Magnesium Sulfate During the Postpartum in Women With Severe Preeclampsia (MAG-PIP)
Primary Purpose
Post Partum Severe Preeclampsia
Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Magnesium Sulfate
Sponsored by
About this trial
This is an interventional treatment trial for Post Partum Severe Preeclampsia
Eligibility Criteria
Inclusion Criteria:
- Severe preeclampsia or severe preeclampsia aggregated to chronic hypertension with > 24 weeks of gestation treated with 4-6 grams of magnesium sulfate for impregnation with a minimum of 8 hours continuous of magnesium sulfate before delivery
- The study begins to terminate pregnancy
Exclusion Criteria:
- HELLP syndrome
- Eclampsia
- Renal insufficiency
- Diabetes mellitus
- Disease of collagen
- Heart disease
Sites / Locations
- Hospital Materno Infantil san Lorezo de las Minas
- Hospital Universitario Maternidad Nuestra señoa de Alta Gracia
- Hospital Teodoro Maldonado De Guayaquil
- Hospital Primero de Mayo
- Hospital Jose Domingo De Obaldia
- Complejo Hospitalario Caja de Seguro Social
- Hospital Santo Tomás
- Hospital Regional de Cojamarca, Perú,
- Instituto Materno perinatal, Maternidad de Lima
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Postpartum Magnesium sulfate
No postpartum treatment
Arm Description
The patient will receive magnesium sulfate as usual for 24 hours postpartum
The patient did not receive postpartum magnesium sulfate or other anticonvulsant during 24 hours postpartum
Outcomes
Primary Outcome Measures
Eclampsia
Convulsion after delivery in any group (with magnesium sulfate or without magnesium sulfate), during 24 hours postpartum.
Secondary Outcome Measures
Postpartum hemorrhage
Blood loss > 500 post vaginal delivery or > 800 cc post cesarean section, during 24 hours postpartum
Maternal respiratory distress
clinical respiratory distress,during 24 hours postpartum
Grams of magnesium sulfate before delivery
Hours and grams of magnesium sulfate before delivery
Severe hypertension postpartum
Diastolic Blood pressure > 110 mmHg and/or systolic blood pressure > 160 mmHg
Full Information
NCT ID
NCT02307201
First Posted
November 24, 2014
Last Updated
January 31, 2017
Sponsor
Complejo Hospitalario Dr. Arnulfo Arias Madrid
1. Study Identification
Unique Protocol Identification Number
NCT02307201
Brief Title
Magnesium Sulfate During the Postpartum in Women With Severe Preeclampsia
Acronym
MAG-PIP
Official Title
Magnesium Sulfate During the Postpartum in Women With Severe Preeclampsia Receiving Treatment for More Than 8 Hours Before Delivery. A Randomized Multicenter Clinical Trial .
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
December 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Complejo Hospitalario Dr. Arnulfo Arias Madrid
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
There is no evidence that patients receiving magnesium sulfate before birth are required to maintain the drug for 24 hours. Therefore the investigators will have a randomized clinical study in patients with severe preeclampsia who have been treated with impregnation of magnesium sulphate and at least eight hours have received the drug before birth. If the patient agrees and signs the consent is randomized to: 1-receive sulfate for 24 hours postpartum as usual or, 2- not receiving the postpartum magnesium sulfate or other anticonvulsant drugs. This study can be conducted in 12 maternity latin america.
Detailed Description
The final treatment known for pre-eclampsia and eclampsia is the termination of pregnancy. However to prevent eclampsia in patients with severe pre-eclampsia has been demonstrated the effectiveness of magnesium sulfate. There are multiple studies that prove the effectiveness of magnesium sulfate to prevent eclampsia in patients with severe disorder of blood pressure during pregnancy. These studies used the drug before birth and continue after birth. Therefore the investigators can not conclude whether the administration just before pregnancy is sufficient to prevent seizure. If the cure or definitive treatment of pre-eclampsia is the interruption, did not seem necessary to justify the administration of drugs anti-eclampsia after birth. Obvious post delivery management with magnesium sulfate arises from the large number of postpartum eclampsia reported in many studies. It is unknown whether administration of magnesium sulfate for a minimum period before delivery, requires even keep the drug post partum.
In addition to magnesium sulfate postpartum, is necessary to maintain urinary catheter to monitoring the removal of magnesium sulfate; is usual to maintain the patient at all or almost all rest by monitoring sulfate and diuresis , this prevents a proper relationship mother and babe and even prevents breastfeeding during that period and is also known increased risk of secondary thromboembolism due to prolonged rest in the postpartum / caesarean section.Thus, maintain magnesium sulfate for 24 hours carries a higher cost, greater vigilance and some risks, without known real effect.
A randomized clinical study conducted by Belfort and colleagues and published in January 2003, where magnesium sulphate compared to nimodipine to prevent eclampsia in women with severe pre-eclampsia, showed interesting outcome. Such research analyzed 819 randomized patients in the nimodipine group and 831 in the magnesium sulfate group. Magnesium sulphate was better than Nimodipine in preventing eclampsia. Interestingly, the greater effectiveness of sulfate appears to prevent all eclampsia postpartum (9 vs 0) and obviously was used before the termination of pregnancy, however no difference compared with nimodipine in eclampsia before birth (12 vs 7).
There are two possible reasons for the non-appearance of postpartum eclampsia: 1- maintain postpartum magnesium sulfate, 2- dose 12-13 grams before birth disruption are sufficient to prevent eclampsia.
The MAGPIE study randomized 1335 postpartum patients (unused sulphate before delivery) using magnesium sulfate postpartum / cesarean (696 women) or placebo postpartum / cesarean (639 women), and found no significant difference in the amount of eclampsia . Thus, the use of magnesium sulfate for first time in the postpartum is not better to use a placebo. If the investigators combine the findings of eclampsia postpartum Belfort study and MAGPIE study is logical to think that the success of the Belfort study in the postpartum is not for the use of magnesium sulfate post delivery and not only due to the termination of pregnancy because there are postpartum eclampsia in the nimodipine group.
If the investigators consider unjustified use of magnesium sulfate postpartum, when maintained at least 8 hours before delivery, the investigators decided to make a non-inferiority randomized study.The investigators assume that using or not using magnesium sulfate during the postpartum prevents similar amount of postpartum eclampsia, if during pregnancy was used (impregnation and at least 8 hours before birth).
For all these reasons the investigators propose the following: A randomized trial is necessary where all those patients who received magnesium sulfate for at least 8 hours before birth (involves impregnation and maintenance 8 hours) will be randomized to two groups of study: 1- Continue magnesium sulfate for 24 hours and 2-not use magnesium sulfate or other anticonvulsant drug post delivery.
This study is planned in 12 maternity latin america
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Partum Severe Preeclampsia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1114 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Postpartum Magnesium sulfate
Arm Type
Experimental
Arm Description
The patient will receive magnesium sulfate as usual for 24 hours postpartum
Arm Title
No postpartum treatment
Arm Type
No Intervention
Arm Description
The patient did not receive postpartum magnesium sulfate or other anticonvulsant during 24 hours postpartum
Intervention Type
Drug
Intervention Name(s)
Magnesium Sulfate
Other Intervention Name(s)
No postpartum treatment
Intervention Description
The patient will receive magnesium sulfate for 24 hours postpartum
Primary Outcome Measure Information:
Title
Eclampsia
Description
Convulsion after delivery in any group (with magnesium sulfate or without magnesium sulfate), during 24 hours postpartum.
Time Frame
24 hours postpartum
Secondary Outcome Measure Information:
Title
Postpartum hemorrhage
Description
Blood loss > 500 post vaginal delivery or > 800 cc post cesarean section, during 24 hours postpartum
Time Frame
24 hours postpartum
Title
Maternal respiratory distress
Description
clinical respiratory distress,during 24 hours postpartum
Time Frame
24 hours postpartum
Title
Grams of magnesium sulfate before delivery
Description
Hours and grams of magnesium sulfate before delivery
Time Frame
8 to 72 hours with magnesium sulfate before delivery
Title
Severe hypertension postpartum
Description
Diastolic Blood pressure > 110 mmHg and/or systolic blood pressure > 160 mmHg
Time Frame
72 hours postdelivery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Severe preeclampsia or severe preeclampsia aggregated to chronic hypertension with > 24 weeks of gestation treated with 4-6 grams of magnesium sulfate for impregnation with a minimum of 8 hours continuous of magnesium sulfate before delivery
The study begins to terminate pregnancy
Exclusion Criteria:
HELLP syndrome
Eclampsia
Renal insufficiency
Diabetes mellitus
Disease of collagen
Heart disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paulino Vigil De Gracia
Organizational Affiliation
Complejo Hospitalario Dr. Arnulfo Arias Madrid
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jack Ludmir, MD
Organizational Affiliation
School of medicine, Pennsylvania Hospital. University de Pennsylvania. Philadelphia
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital Materno Infantil san Lorezo de las Minas
City
Santo Domingo
Country
Dominican Republic
Facility Name
Hospital Universitario Maternidad Nuestra señoa de Alta Gracia
City
Santo Domingo
Country
Dominican Republic
Facility Name
Hospital Teodoro Maldonado De Guayaquil
City
Guayaquil
Country
Ecuador
Facility Name
Hospital Primero de Mayo
City
San Salvador
Country
El Salvador
Facility Name
Hospital Jose Domingo De Obaldia
City
Chiriqui
ZIP/Postal Code
507
Country
Panama
Facility Name
Complejo Hospitalario Caja de Seguro Social
City
Panamá
ZIP/Postal Code
507
Country
Panama
Facility Name
Hospital Santo Tomás
City
Panamá
ZIP/Postal Code
507
Country
Panama
Facility Name
Hospital Regional de Cojamarca, Perú,
City
Cajamarca
Country
Peru
Facility Name
Instituto Materno perinatal, Maternidad de Lima
City
Lima
Country
Peru
12. IPD Sharing Statement
Citations:
PubMed Identifier
12540643
Citation
Belfort MA, Anthony J, Saade GR, Allen JC Jr; Nimodipine Study Group. A comparison of magnesium sulfate and nimodipine for the prevention of eclampsia. N Engl J Med. 2003 Jan 23;348(4):304-11. doi: 10.1056/NEJMoa021180.
Results Reference
background
PubMed Identifier
12057549
Citation
Altman D, Carroli G, Duley L, Farrell B, Moodley J, Neilson J, Smith D; Magpie Trial Collaboration Group. Do women with pre-eclampsia, and their babies, benefit from magnesium sulphate? The Magpie Trial: a randomised placebo-controlled trial. Lancet. 2002 Jun 1;359(9321):1877-90. doi: 10.1016/s0140-6736(02)08778-0.
Results Reference
result
Learn more about this trial
Magnesium Sulfate During the Postpartum in Women With Severe Preeclampsia
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