Comparison · NCT05890586-385bbda3
Arm B - Fluvoxamine 50 vs Arm B - Placebo: Number of Participants With Mortality
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. Arm B - Fluvoxamine 50 vs Arm B - Placebo: Number of Participants With Mortality. Trial comparisons, record NCT05890586-385bbda3. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05890586-385bbda3
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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 | 0.00591 | wilson | |
| Risk in group 2 | 0 | 0.000000000000000000434 | 0.00656 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.00656 | 0.00591 | 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 treat | from the risk difference interval | the two groups' risks are equal |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Arm B - Fluvoxamine 50 | Fluvoxamine will be self-administered orally by each participant at a dose of 50 mg twice a day for 10 days.~Fluvoxamine: Fluvoxamine is a round golden 50 mg tablet that is scored on both sides - one side has APO and the other side has F50 with a partial bisect. All packaging will be labeled to indicate that the product is for investigational use, administered at a dose of 50 mg, twice daily for 10 days. | 0 | 646 | OG000 |
| Group 2 | Arm B - Placebo | Placebo - appearance and size matched to active study drug. Placebo will be self-administered orally by each participant twice a day for 10 days.~Placebo: Each study arm will contain a placebo comparator. Placebo will look similar to study drug and will be administered via the same route of administration and dose. However, placebo will be an inactive substance, containing no study drug. | 0 | 582 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Mortality
- Description
- Time frame
- Up to 28 days
- Population
- Data not collected on one participant.
Source ClinicalTrials.gov
Trial
- Title
- ACTIV-6: COVID-19 Study of Repurposed Medications - Arm B (Fluvoxamine)
- NCT number
- NCT05890586
- Phases
- PHASE3
- Conditions
- Covid19
- Interventions
- Fluvoxamine, Placebo
- Lead sponsor
- Susanna Naggie, MD
- Results first posted
- 2023-08-02
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT05890586?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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