Trial · NCT01075243
Results by group45
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 45
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) | Paracetamol Caplet 1000mg | 16.08 | Standard Deviation 10.68 | Score on a scale | |
| Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) | Paracetamol Caplet 650 mg | 12.42 | Standard Deviation 9.89 | Score on a scale | |
| Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) | Placebo Caplet | 4.63 | Standard Deviation 8.82 | Score on a scale | |
| Time to Confirmed First Perceptible Relief | Paracetamol Caplet 1000mg | 54.72 | Standard Deviation 104.911 | minutes | |
| Time to Confirmed First Perceptible Relief | Paracetamol Caplet 650 mg | 69.67 | Standard Deviation 120.501 | minutes | |
| Time to Confirmed First Perceptible Relief | Placebo Caplet | 225.70 | Standard Deviation 162.884 | minutes | |
| Time to Onset of Meaningful Pain Relief | Paracetamol Caplet 1000mg | 70.53 | Standard Deviation 101.474 | minutes | |
| Time to Onset of Meaningful Pain Relief | Paracetamol Caplet 650 mg | 88.16 | Standard Deviation 115.955 | minutes | |
| Time to Onset of Meaningful Pain Relief | Placebo Caplet | 247.14 | Standard Deviation 143.028 | minutes | |
| Time to Start Using Rescue Medication | Paracetamol Caplet 1000 mg | 360.00 | Full Range 124.00 to 360.00 | minutes | |
| Time to Start Using Rescue Medication | Paracetamol Caplet 650 mg | 314.00 | Full Range 123.00 to 360.00 | minutes | |
| Time to Start Using Rescue Medication | Placebo Caplet | 131.00 | Full Range 115.00 to 360.00 | minutes | |
| Percentage of Participants Who Took Rescue Medication at 2 Hours | Paracetamol Caplet 1000mg | 0.00 | Percentage of participants | ||
| Percentage of Participants Who Took Rescue Medication at 2 Hours | Paracetamol Caplet 650 mg | 0.00 | Percentage of participants | ||
| Percentage of Participants Who Took Rescue Medication at 2 Hours | Placebo Caplet | 1.30 | Percentage of participants | ||
| Percentage of Participants Who Took Rescue Medication at 6 Hours | Paracetamol Caplet 1000mg | 44.20 | Percentage of participants | ||
| Percentage of Participants Who Took Rescue Medication at 6 Hours | Paracetamol Caplet 650 mg | 51.90 | Percentage of participants | ||
| Percentage of Participants Who Took Rescue Medication at 6 Hours | Placebo Caplet | 70.00 | Percentage of participants | ||
| SPRID at 2 Hours | Paracetamol Caplet 1000mg | 6.49 | Standard Deviation 3.11 | Score on a scale | |
| SPRID at 2 Hours | Paracetamol Caplet 650 mg | 5.57 | Standard Deviation 2.94 | Score on a scale |
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/NCT01075243/results