Trial · NCT04066023
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Percentage of Subjects Who Achieve Pain Relief | 15 minutes | Pain relief is defined by a decrease in pain from severe to mild or none without the use of acute rescue medication. |
| Primary | Percentage of Subjects Who Achieve Sustained Pain Relief | 15 minutes to 60 minutes | Sustained pain relief requires a pain rating of mild or none at each timepoint from 15 minutes to 60 minutes without the use of acute rescue medication. |
| Secondary | Percentage of Subjects That Achieve Pain Relief | 5 minutes | Pain relief is defined by a decrease in pain from severe to mild or none without the use of acute rescue medication. |
| Secondary | Percentage of Subjects That Achieve Sustained Pain Relief | 5 minutes to 60 minutes | Sustained pain relief requires a pain rating of mild or none at each timepoint within the time frame without the use of acute rescue medication. |
| Secondary | Percentage of Subjects That Achieve Pain Freedom | 10 minutes | Pain freedom is defined by a decrease in pain from severe to none without the use of acute rescue medication. |
| Secondary | Percentage of Subjects That Achieve Sustained Pain Freedom | 15 to 60 minutes | Sustained pain freedom requires a pain rating of none at each timepoint within the time frame without the use of acute rescue medication. |
| Secondary | Percentage of Subjects Able to Perform Their Usual Daily Activities as Assessed by the Subject | within 20 minutes | Whether or not subjects were able to perform their usual daily activities was assessed by subject responses (Yes or No) in the electronic diary (eDiary) to the question, "Do you feel able to perform your usual daily activities?" If a subject responded "Yes" but had used a rescue medication, the subject was considered as not being able to perform the usual daily activities. |
| Secondary | Percentage of Subjects That Achieve Pain Relief | 10 minutes | Pain relief is defined by a decrease in pain from severe to mild or none without the use of acute rescue medication |
| Secondary | Percentage of Subjects That Achieve Pain Relief | 20 minutes | Pain relief is defined by a decrease in pain from severe to mild or none without the use of acute rescue medication. |
| Secondary | Percentage of Subjects That Achieve Sustained Pain Relief | 10 minutes to 60 minutes | Sustained pain relief requires a pain rating of mild or none at each timepoint within the time frame without the use of acute rescue medication. |
| Secondary | Percentage of Subjects That Achieve Pain Freedom | 20 minutes | Pain freedom is defined by a decrease in pain from severe to none without the use of acute rescue medication. |
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/NCT04066023/registered