Comparison · NCT00599339-sae
Associated With Rotigotine vs Not Associated With Rotigotine: 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. Associated With Rotigotine vs Not Associated With Rotigotine: serious adverse events. Trial comparisons, record NCT00599339-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00599339-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 | 0.188 | 0.168 | 0.209 | wilson | |
| Risk in group 2 | 0.203 | 0.182 | 0.225 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0148 | -0.0446 | 0.015 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.927 | 0.796 | 1.08 | log | |
| Odds ratio, group 1 over group 2 | 0.91 | 0.753 | 1.1 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Associated With Rotigotine than on Not Associated With Rotigotine | 67.6 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Associated With Rotigotine | A patient was analyzed related to Adverse Events (AEs) associated with Rotigotine only if during the study he was at risk to develop an AE associated with Rotigotine.~An Adverse Event was considered to be associated with Rotigotine if Rotigotine was administered at least once within 30 days prior to the onset of the adverse event. Associated Event does not necessarily mean related to treatment with Rotigotine. | 261 | 1,390 | EG000 |
| Group 2 | Not Associated With Rotigotine | A patient was analyzed related to Adverse Events (AEs) not associated with Rotigotine only if during the study he was at risk to develop an AE not associated with Rotigotine.~An adverse event was considered not to be associated with Rotigotine, if no Rotigotine was administered in the 30 days period prior to the onset of the AE. | 269 | 1,328 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse Events (AEs) were collected during the course of the study from Baseline (Visit 1) up to Visit 7 (Month 33 ± 30 days).
Source ClinicalTrials.gov
Trial
- Title
- Transdermal Rotigotine User Surveillance Study
- NCT number
- NCT00599339
- Phases
- Conditions
- Idiopathic Parkinson Disease
- Interventions
- Lead sponsor
- UCB Pharma
- Results first posted
- 2015-04-29
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00599339?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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