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Trial · NCT02835339

Magnesium Sulfate in Obese Preeclamptics

NCT02835339, Phase 4, Completed, Oregon Health and Science University; results first posted 2020-05-13

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Magnesium Sulfate in Obese Preeclamptics. Trials, record NCT02835339. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02835339

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Magnesium Sulfate in Obese Preeclamptics
NCT number
NCT02835339
Status
Completed
Phases
Phase 4
Enrollment
66 participants, actual
Lead sponsor
Oregon Health and Science University
Conditions
Preeclampsia
Interventions
Magnesium sulfate 4g loading dose, 1g/hr infusion, Magnesium sulfate 6g loading dose, 2g/hr infusion
First posted
2016-07-18
Last updated
2020-05-13
Results first posted
2020-05-13

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMaternal Serum Magnesium Level at 4 Hours After Administration4 hoursmagnesium level in mg/dL
SecondaryMaternal Serum Magnesium Level at Time of DeliveryWithin 20 minutes of deliverymagnesium level in mg/dL
SecondaryMaternal Side Effects4 hoursPresence or absence of the following: flushing, lethargy, palpitations, pain at IV site, respiratory depression

Outcomes3

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMaternal Serum Magnesium Level at 4 Hours After Administration4 hoursmg/dLMEAN
SECONDARYMaternal Serum Magnesium Level at Time of DeliveryWithin 20 minutes of deliverymg/dLMEAN
SECONDARYMaternal Side Effects4 hourspercentage of participantsNUMBER

Results by group16

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Maternal Serum Magnesium Level at 4 Hours After AdministrationMgSO4 4g Load, 1g/hr Infusion3.53Standard Deviation .3mg/dL
Maternal Serum Magnesium Level at 4 Hours After AdministrationMgSO4 6g Load, 2g/hr Infusion4.41Standard Deviation .5mg/dL
Maternal Serum Magnesium Level at Time of DeliveryMgSO4 4g Load, 1g/hr Infusion3.73Standard Deviation 0.7mg/dL
Maternal Serum Magnesium Level at Time of DeliveryMgSO4 6g Load, 2g/hr Infusion5.44Standard Deviation 1.0mg/dL
Maternal Side EffectsMgSO4 4g Load, 1g/hr InfusionNausea5.5percentage of participants
Maternal Side EffectsMgSO4 6g Load, 2g/hr InfusionNausea10.5percentage of participants
Maternal Side EffectsMgSO4 4g Load, 1g/hr InfusionFlushing0percentage of participants
Maternal Side EffectsMgSO4 6g Load, 2g/hr InfusionFlushing5.2percentage of participants
Maternal Side EffectsMgSO4 4g Load, 1g/hr InfusionLethargy0percentage of participants
Maternal Side EffectsMgSO4 6g Load, 2g/hr InfusionLethargy0percentage of participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMgSO4 4g Load, 1g/hr Infusion31
Overall StudySTARTEDMgSO4 6g Load, 2g/hr Infusion35
Overall StudyCOMPLETEDMgSO4 4g Load, 1g/hr Infusion18
Overall StudyCOMPLETEDMgSO4 6g Load, 2g/hr Infusion19
Overall StudyNOT COMPLETEDMgSO4 4g Load, 1g/hr Infusion13
Overall StudyNOT COMPLETEDMgSO4 6g Load, 2g/hr Infusion16

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMgSO4 4g Load, 1g/hr Infusion018
Total, all-cause mortalityMgSO4 6g Load, 2g/hr Infusion019
Total, other adverse eventsMgSO4 4g Load, 1g/hr Infusion018
Total, other adverse eventsMgSO4 6g Load, 2g/hr Infusion019
Total, serious adverse eventsMgSO4 4g Load, 1g/hr Infusion018
Total, serious adverse eventsMgSO4 6g Load, 2g/hr Infusion019

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
33156201DERIVEDPubMed
37815037DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
MgSO4 4g Load, 1g/hr Infusion vs MgSO4 6g Load, 2g/hr Infusion: deaths from any causeTrial comparisons
MgSO4 4g Load, 1g/hr Infusion vs MgSO4 6g Load, 2g/hr Infusion: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02835339

GET https://conductscience.org/api/trials/v1/NCT02835339/registered