Comparison · NCT01799213-sae
Meloxicam vs Placebo: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Meloxicam vs Placebo: serious adverse events. Trial comparisons, record NCT01799213-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01799213-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0217 | 0.00849 | 0.0546 | wilson | |
| Risk in group 2 | 0.0167 | 0.00568 | 0.0478 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00507 | -0.0288 | 0.0397 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.3 | 0.296 | 5.75 | log | |
| Odds ratio, group 1 over group 2 | 1.31 | 0.289 | 5.94 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Meloxicam than on Placebo | 197 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Meloxicam | Participants in Meloxicam Arm | 4 | 184 | EG001 |
| Group 2 | Placebo | Participants in Placebo (CBT) Arm | 3 | 180 | EG000 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Adverse event data were collected through study completion, an average of 14 weeks. After 2-week run-in period where all subjects replaced their current NSAID with the study drug (meloxicam 15mg per day), remaining eligible subjects participated in 4-week, double-blind, placebo-controlled, non-inferiority randomized withdrawal trial (RWT). After 4 weeks, subjects in the meloxicam arm continued study drug. Subjects in the placebo arm stopped the placebo and participated in a 10-week CBT program.
Source ClinicalTrials.gov
Trial
- Title
- Discontinuing NSAIDs in Veterans With Knee Osteoarthritis
- NCT number
- NCT01799213
- Phases
- PHASE2
- Conditions
- Knee Osteoarthritis
- Interventions
- Meloxicam 15 mg po QD, Cognitive Behavioral Therapy
- Lead sponsor
- VA Office of Research and Development
- Results first posted
- 2019-12-16
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01799213?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
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
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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