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Trial · NCT05967442

Magnesium Versus Prochlorperazine Versus Metoclopramide for Migraines

NCT05967442, Phase 3, Completed, Wake Forest University Health Sciences; results first posted 2024-10-01

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Magnesium Versus Prochlorperazine Versus Metoclopramide for Migraines. Trials, record NCT05967442. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05967442

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Trial

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

Title
Magnesium Versus Prochlorperazine Versus Metoclopramide for Migraines
NCT number
NCT05967442
Status
Completed
Phases
Phase 3
Enrollment
157 participants, actual
Lead sponsor
Wake Forest University Health Sciences
Conditions
Migraine, Headache
Interventions
Magnesium Sulfate, Metoclopramide 10mg, Prochlorperazine (Compazine) Injection
First posted
2023-08-01
Last updated
2024-10-08
Results first posted
2024-10-01

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
Primary30 Minute Pain Score30 minutes after initiationScores range from 0-10. A higher score, denotes more pain
SecondaryLength of StayFrom time of arrival to time of discharge.Emergency Department Length of stay. Measured from time of arrival to time of discharged documented in the electronic medical record.
SecondaryNeed for Rescue AnalgesiaFrom time of arrival to time of discharge.Percentage of participants who had necessity for rescue analgesics after study drug administration

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARY30 Minute Pain Score30 minutes after initiationFull cohortscore on a scaleMEDIAN
SECONDARYLength of StayFrom time of arrival to time of discharge.minutesMEDIAN
SECONDARYNeed for Rescue AnalgesiaFrom time of arrival to time of discharge.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group9

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

OutcomeGroupCategoryValueSpreadUnits
30 Minute Pain ScoreMagnesium3Inter-Quartile Range 1 to 4score on a scale
30 Minute Pain ScoreMetoclopramide3Inter-Quartile Range 1 to 4score on a scale
30 Minute Pain ScoreProchlorperazine3Inter-Quartile Range 1 to 5score on a scale
Length of StayMagnesium325Inter-Quartile Range 274 to 410minutes
Length of StayMetoclopramide308Inter-Quartile Range 263.5 to 403minutes
Length of StayProchlorperazine332Inter-Quartile Range 268.5 to 391minutes
Need for Rescue AnalgesiaMagnesium26Participants
Need for Rescue AnalgesiaMetoclopramide15Participants
Need for Rescue AnalgesiaProchlorperazine17Participants

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMagnesium61
Overall StudySTARTEDMetoclopramide44
Overall StudySTARTEDProchlorperazine52
Overall StudyCOMPLETEDMagnesium61
Overall StudyCOMPLETEDMetoclopramide44
Overall StudyCOMPLETEDProchlorperazine52
Overall StudyNOT COMPLETEDMagnesium0
Overall StudyNOT COMPLETEDMetoclopramide0
Overall StudyNOT COMPLETEDProchlorperazine0

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 totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMagnesium061
Total, all-cause mortalityMetoclopramide044
Total, all-cause mortalityProchlorperazine052
Total, other adverse eventsMagnesium061
Total, other adverse eventsMetoclopramide044
Total, other adverse eventsProchlorperazine052
Total, serious adverse eventsMagnesium061
Total, serious adverse eventsMetoclopramide044
Total, serious adverse eventsProchlorperazine052

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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 comparisons0

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

None in this release.

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/NCT05967442

GET https://conductscience.org/api/trials/v1/NCT05967442/registered