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Trial · NCT00682734

Metoclopramide for Migraine: A Dose Finding Study

NCT00682734, Phase 3, Completed, Montefiore Medical Center; results first posted 2012-12-31

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Metoclopramide for Migraine: A Dose Finding Study. Trials, record NCT00682734. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00682734

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Trial

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

Title
Metoclopramide for Migraine: A Dose Finding Study
NCT number
NCT00682734
Status
Completed
Phases
Phase 3
Enrollment
349 participants, actual
Lead sponsor
Montefiore Medical Center
Conditions
Migraine
Interventions
metoclopramide, metoclopramide, metoclopramide, Diphenhydramine 25mg
First posted
2008-05-22
Last updated
2018-05-31
Results first posted
2012-12-31

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryPain Intensity ScoreBaseline, 60 minutes
Change in 11 point pain intensity score between baseline and one hour. At both baseline and one hour, all patients were asked to describe their pain on a scale from 0 to 10, with 0 signifying no pain and 10 signifying the worst pain imaginable. Therefore, the CHANGE in pain score could range from -10 through 10.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPain Intensity ScoreBaseline, 60 minutesper protocolscores on a scaleMEAN

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Pain Intensity ScoreMetoclopramide 10 mg Intravenous4.7Standard Deviation 2.6scores on a scale
Pain Intensity ScoreMetoclopramide 20 mg4.9Standard Deviation 2.8scores on a scale
Pain Intensity ScoreMetoclopramide 40 mg5.3Standard Deviation 2.8scores on a scale

Participant flow18

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

PeriodMilestoneGroupParticipantsUnits counted
Emergency Department PortionSTARTEDMetoclopramide 10 mg Intravenous113
Emergency Department PortionSTARTEDMetoclopramide 20 mg Intravenous118
Emergency Department PortionSTARTEDMetoclopramide 40 mg Intravenous118
Emergency Department PortionCOMPLETEDMetoclopramide 10 mg Intravenous113
Emergency Department PortionCOMPLETEDMetoclopramide 20 mg Intravenous117
Emergency Department PortionCOMPLETEDMetoclopramide 40 mg Intravenous117
Emergency Department PortionNOT COMPLETEDMetoclopramide 10 mg Intravenous0
Emergency Department PortionNOT COMPLETEDMetoclopramide 20 mg Intravenous1
Emergency Department PortionNOT COMPLETEDMetoclopramide 40 mg Intravenous1
48 Hour Follow-upSTARTEDMetoclopramide 10 mg Intravenous113

Adverse events6

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAkathisiaNervous system disordersMetoclopramide 10 mg Intravenous8113
otherAkathisiaNervous system disordersMetoclopramide 20 mg8118
otherAkathisiaNervous system disordersMetoclopramide 40 mg7118
seriousEncephalitisNervous system disordersMetoclopramide 10 mg Intravenous01130
seriousEncephalitisNervous system disordersMetoclopramide 20 mg11181
seriousEncephalitisNervous system disordersMetoclopramide 40 mg01180

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMetoclopramide 10 mg Intravenous
Total, all-cause mortalityMetoclopramide 20 mg
Total, all-cause mortalityMetoclopramide 40 mg
Total, other adverse eventsMetoclopramide 10 mg Intravenous8113
Total, other adverse eventsMetoclopramide 20 mg8118
Total, other adverse eventsMetoclopramide 40 mg7118
Total, serious adverse eventsMetoclopramide 10 mg Intravenous0113
Total, serious adverse eventsMetoclopramide 20 mg1118
Total, serious adverse eventsMetoclopramide 40 mg0118

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/NCT00682734

GET https://conductscience.org/api/trials/v1/NCT00682734/registered