Trial · NCT02439320
Outcomes12
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Percentage of Participants Who Are Headache Pain Free | 2 hours post dose | All randomized participants who received at least one dose of study drug and had evaluable headache pain free data. | percentage of participants | NUMBER |
| PRIMARY | Percentage of Participants Who Are Most Bothersome Symptom (MBS) Free | 2 hours post dose | All randomized participants who received at least one dose of study drug and had evaluable MBS data. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Who Have Headache Relief After First Dose | 2 hours post dose | All randomized participants who received at least one dose of study drug and had evaluable headache relief data. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants With Headache Recurrence | From 2 hours post dose up to 48 hours | Randomized participants who received a dose of study drug and had postdose headache severity or symptom assessments. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Who Used Rescue Medication | 2 hours post dose | Randomized participants who received a dose of study drug and had postdose headache severity or symptom assessments. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Who Used Rescue Medication | Anytime between 2-24 hours post dose | Randomized participants who received a dose of study drug and had postdose headache severity or symptom assessments. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Who Used Rescue Medication | Anytime 24-48 hours post dose | All randomized participants who received at least one dose of study drug and had evaluable use of rescue medication data. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Nausea Free | 2 hours post dose | All randomized participants who used at least 1 dose of study drug and had any post-dose headache severity or symptom assessments. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Phonophobia Free | 2 hours post dose | All randomized participants who used at least 1 dose of study drug and had any post-dose headache severity or symptom assessments. | percentage of participants | NUMBER |
| SECONDARY | Percentage of Participants Photophobia Free | 2 hours post dose | All randomized participants who received at least one dose of study drug and had evaluable photophobia free data. | percentage of participants | NUMBER |
| SECONDARY | Participants With Serious Adverse Events (SAE) | Baseline up to 11 weeks | All randomized participants who had received at least one dose of study drug. Results are displayed by the first dose taken. | Participants | COUNT_OF_PARTICIPANTS |
| OTHER_PRE_SPECIFIED | Percentage of Participants With Resource Utilization | 6 months prior to enrolling in study to end of study (Up to 11 Weeks) within 7 days of treating a single migraine attack | All randomized participants who used at least 1 dose of study drug, regardless of whether or not they underwent any study assessments. | percentage of participants | NUMBER |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
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GET https://conductscience.org/api/trials/v1/NCT02439320/outcomes