Trial · NCT01426971
Ibuprofen Versus Ibuprofen Plus Caffeine in the Treatment of Migraine.
NCT01426971, Phase 3, Withdrawn, Sanofi
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Ibuprofen Versus Ibuprofen Plus Caffeine in the Treatment of Migraine. Trials, record NCT01426971. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01426971
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Ibuprofen Versus Ibuprofen Plus Caffeine in the Treatment of Migraine.
- NCT number
- NCT01426971
- Status
- Withdrawn
- Phases
- Phase 3
- Enrollment
- 0 participants, actual
- Lead sponsor
- Sanofi
- Conditions
- Pain
- Interventions
- IBUPROFEN + CAFFEINE, IBUPROFEN
- First posted
- 2011-09-01
- Last updated
- 2012-11-27
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of patients with reduction of at least 30mm in the visual scale (VAS) of pain | from baseline to 60 minutes | |
| Secondary | Number of patients with more than 50% of pain reduction | up to 45 minutes | |
| Secondary | Median time of the first perception of pain relief since study medication intake | 4 hours | |
| Secondary | Median time to onset of significant pain relief compared to the time of study medication intake | 4 hours | |
| Secondary | Headache Relief Rating score (HRR) | up to 60 mins | |
| Secondary | Mean of VAS difference between each time after medication intake and the baseline. | 15, 30, 45, 60, 120 and 240 minutes post dose | |
| Secondary | Number of patients who used the third tablet of study medication | up to 24 hours | |
| Secondary | Number of patients requiring rescue medication | up to 24 hours |
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.
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.
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/NCT01426971
GET https://conductscience.org/api/trials/v1/NCT01426971/registered