Trial · NCT02646566
Outcomes11
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Complete Response (Success of Initial PONV Treatment) | 0-24 hours after administration of study medication | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Complete Response 0-2 Hrs | 0-2 hours after administration of study medication | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Complete Response 0-4 Hrs | 0-4 hours after administration of study medication | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Complete Response 0-6 Hrs | 0-6 hours after administration of study medication | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Time to Treatment Failure | 0-24 hours after study drug administration | Modified ITT population | minutes | MEDIAN |
| SECONDARY | Number of Patients With Incidence of Emesis | 30 mins to 24 hours after study drug administration | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Patients Receiving Rescue Medication | 0-24 hours after study drug administration | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Patients With an Incidence of Significant Nausea | 30 mins to 24 hours after study drug administration | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Patients With an Incidence of Nausea | 30 mins to 24 hours after drug administration | Modified ITT population | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Maximum Severity of Nausea | 30 mins to 24 hours after study drug administration | Modified ITT population | Score on a scale | MEAN |
| SECONDARY | Evolution Score of Nausea (0-180 Mins) | 0-180 minutes after study drug administration | Modified ITT population | Score on a scale*min | MEAN |
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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02646566/outcomes