Trial · NCT05983354
Oral Medications for the Management of Acute Migraine Headache in the Emergency Department
NCT05983354, Not applicable, Withdrawn, Health Sciences North Research Institute
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Oral Medications for the Management of Acute Migraine Headache in the Emergency Department. Trials, record NCT05983354. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05983354
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Oral Medications for the Management of Acute Migraine Headache in the Emergency Department
- NCT number
- NCT05983354
- Status
- Withdrawn
- Phases
- Not applicable
- Enrollment
- 0 participants, actual
- Lead sponsor
- Health Sciences North Research Institute
- Conditions
- Acute Migraine Headache
- Interventions
- Oral metoclopramide and ibuprofen, Intravenous metoclopramide and ketorolac
- First posted
- 2023-08-09
- Last updated
- 2026-10-05
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Recruitment rate | 6 months | Proportion of eligible patients presenting to ED who are successfully recruited |
| Primary | Pain relief | 60 minutes | Change in visual analogue scale (0-10 where 0 is no pain and 10 is maximal pain) from baseline to 60 minutes after medication administration |
| Secondary | Proportion of eligible patients approached | 6 months | Proportion of all eligible patients who were approached by research assistants |
| Secondary | Rate of attrition during the study period | 24 hours | Number of patients recruited to study who ended participation during study period |
| Secondary | Pain relief at 2 hours | 120 minutes | Change in visual analogue scale from baseline to 120 minutes after medication administration |
| Secondary | Freedom from headache | 60 minutes | Patients who report complete resolution of headache at 60 minutes from medication administration |
| Secondary | Need for rescue medication | 24 h | Additional medications administered by treating physician after 60 minutes |
| Secondary | Emergency department length of stay | 24 hours | Time from initial physician assessment to discharge |
| Secondary | Return to emergency department | 24 hours | Patients who were registered again to the ED within 24 hours of discharge |
| Secondary | Adverse reactions | 24 hours | Any adverse reaction reported during the study period |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
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 totals0
The totals the trial posted for each group.
None in this release.
Papers7
The papers the trial lists on ClinicalTrials.gov.
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.
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/NCT05983354
GET https://conductscience.org/api/trials/v1/NCT05983354/registered