Comparison · NCT02329964-sae
R-S Group vs S-C-N Group: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
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ConductScience Library. R-S Group vs S-C-N Group: serious adverse events. Trial comparisons, record NCT02329964-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02329964-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 | 0 | 0.0876 | wilson | |
| Risk in group 2 | 0 | 0 | 0.0876 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.0876 | 0.0876 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | log | a group has no participants with the outcome | |||
| Odds ratio, group 1 over group 2 | log | a cell of the two-by-two table is zero | |||
| Number needed to harm | from the risk difference interval | the two groups' risks are equal |
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 | R-S Group | Rocuronium-Sugammadex group~1. Induction agent :~ * IV Propofol 1.5-2.5 mg/Kg and fentanyl 1.5mcg/kg~2. During induction of anesthesia, as muscle relaxant agent~ * Rocuronium 1mg/kg~3. After endotracheal intubation~ * normal saline(0.025 ml/kg)~4. Additive dose, for ensuring that neuromuscular blockade remains below T2 during surgery~ * Rocuronium 0.15mg/kg~5. Relaxant agent reversal. at the the end of surgery.~ * sugammadex 2mg/kg | 0 | 40 | EG000 |
| Group 2 | S-C-N Group | Succinylcholine-Cisatracurium-Neostigmine group~1. Induction agent :~ * IV Propofol 1.5-2.5 mg/Kg and fentanyl 1.5mcg/kg~2. During induction of anesthesia, as muscle relaxant agent~ * Succinylcholine 1mg/kg~3. After endotracheal intubation,~ * Cisatracurium 0.08mg/kg~4. Additive dose, for ensuring that neuromuscular blockade remains below T2 during surgery~ * Succinylcholine 10mg~5. Relaxant agent reversal. at the appearance of second TOF twitch (T2).~ * Neostigmine 0.2 mg/kg with atropine 10μg/kg (for preventing side effects of neostigmine) | 0 | 40 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
- Effectiveness of Sugammadex in LMS Surgery
- NCT number
- NCT02329964
- Phases
- PHASE4
- Conditions
- Muscle Relaxation
- Interventions
- Sugammadex, Neostigmine
- Lead sponsor
- Korea University Anam Hospital
- Results first posted
- 2015-09-28
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02329964?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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