Trial · NCT00913627
Results by group452
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 452
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Time-weighted Sum of Pain Intensity Difference Score From 0 to 12 Hours (SPID 0-12) | Placebo | 0.05 | Standard Deviation 9.22 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 0 to 12 Hours (SPID 0-12) | Ibuprofen IR/ER (Roller Compaction) | 16.87 | Standard Deviation 9.35 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 0 to 12 Hours (SPID 0-12) | Ibuprofen IR/ER (Wet Granulation) | 17.34 | Standard Deviation 10.54 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 0 to 12 Hours (SPID 0-12) | Naproxen | 12.66 | Standard Deviation 10.02 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 8 to 12 Hours (SPID 8-12) | Placebo | -0.03 | Standard Deviation 4.05 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 8 to 12 Hours (SPID 8-12) | Ibuprofen IR/ER (Roller Compaction) | 6.57 | Standard Deviation 4.44 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 8 to 12 Hours (SPID 8-12) | Ibuprofen IR/ER (Wet Granulation) | 7.14 | Standard Deviation 5.24 | units on a scale | |
| Time-weighted Sum of Pain Intensity Difference Score From 8 to 12 Hours (SPID 8-12) | Naproxen | 5.14 | Standard Deviation 5.02 | units on a scale | |
| Time to First Perceptible Pain Relief | Placebo | NA | 95% Confidence Interval NA to NA | minutes | |
| Time to First Perceptible Pain Relief | Ibuprofen IR/ER (Roller Compaction) | 29.4 | 95% Confidence Interval 23.3 to 35.3 | minutes | |
| Time to First Perceptible Pain Relief | Ibuprofen IR/ER (Wet Granulation) | 29.4 | 95% Confidence Interval 26.1 to 36.2 | minutes | |
| Time to First Perceptible Pain Relief | Naproxen | 32.1 | 95% Confidence Interval 29.5 to 58.0 | minutes | |
| Time to Treatment Failure | Placebo | 1.7 | 95% Confidence Interval 1.7 to 2.2 | hours | |
| Time to Treatment Failure | Ibuprofen IR/ER (Roller Compaction) | NA | 95% Confidence Interval NA to NA | hours | |
| Time to Treatment Failure | Ibuprofen IR/ER (Wet Granulation) | NA | 95% Confidence Interval NA to NA | hours | |
| Time to Treatment Failure | Naproxen | NA | 95% Confidence Interval NA to NA | hours | |
| Percentage of Participants With Treatment Failure | Placebo | 8 hours | 82.8 | percentage of participants | |
| Percentage of Participants With Treatment Failure | Ibuprofen IR/ER (Roller Compaction) | 8 hours | 11.3 | percentage of participants | |
| Percentage of Participants With Treatment Failure | Ibuprofen IR/ER (Wet Granulation) | 8 hours | 12.5 | percentage of participants | |
| Percentage of Participants With Treatment Failure | Naproxen | 8 hours | 24.1 | percentage of participants |
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.
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GET https://conductscience.org/api/trials/v1/NCT00913627/results