Comparison · NCT00733343-00a8dba4
Treatment Group vs Control Group: First Survived Resuscitation of Sudden Cardiac Arrest (Evaluation Will Also be Made by the ERC)
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. Treatment Group vs Control Group: First Survived Resuscitation of Sudden Cardiac Arrest (Evaluation Will Also be Made by the ERC). Trial comparisons, record NCT00733343-00a8dba4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00733343-00a8dba4
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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 | 0.027 | 0.0172 | 0.0423 | wilson | |
| Risk in group 2 | 0.0243 | 0.015 | 0.0391 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00275 | -0.015 | 0.0206 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.11 | 0.573 | 2.16 | log | |
| Odds ratio, group 1 over group 2 | 1.12 | 0.564 | 2.21 | log | |
| Number needed to treat, for one more participant with the outcome on Treatment Group than on Control Group | 364 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: control.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Treatment Group | treatment with Adaptive Servoventilation (Europe: AutoSet CS (USA: VPAP Adapt SV)) + standard medical therapy according to applicable guidelines (ESC, ACC/AHA)~Europe: AutoSet CS (USA: VPAP Adapt SV): At least 3 hours average daily usage time | 18 | 666 | OG000 |
| Group 2 | Control Group | standard medical therapy according to applicable guidelines (ESC, ACC/AHA) | 16 | 659 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- First Survived Resuscitation of Sudden Cardiac Arrest (Evaluation Will Also be Made by the ERC)
- Description
- Time frame
- the last follow up or at the last available observation within FU, assessed for up to 70 weeks
- Population
Source ClinicalTrials.gov
Trial
- Title
- Treatment of Predominant Central Sleep Apnoea by Adaptive Servo Ventilation in Patients With Heart Failure
- NCT number
- NCT00733343
- Phases
- NA
- Conditions
- Heart Failure, Sleep Disordered Breathing
- Interventions
- Europe: AutoSet CS (USA: VPAP Adapt SV)
- Lead sponsor
- ResMed
- Results first posted
- 2020-05-12
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00733343?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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