Comparison · NCT00733980-ac980804
GSK561679 vs Placebo: Number of Participants With Abnormal Hematology Values of PCI-Platelet
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. GSK561679 vs Placebo: Number of Participants With Abnormal Hematology Values of PCI-Platelet. Trial comparisons, record NCT00733980-ac980804. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00733980-ac980804
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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 | 0.055 | wilson | |
| Risk in group 2 | 0.0159 | 0.00281 | 0.0846 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0159 | -0.0846 | 0.0407 | 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, for one fewer participant with the outcome on GSK561679 than on Placebo | 63 | 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 | GSK561679 | The participants in this arm received GSK561679, 350 mg orally daily as 3x100 mg tablets plus one 50 mg tablet in evening, for 6-weeks | 0 | 66 | OG000 |
| Group 2 | Placebo | The participants in this arm received matching placebo, and took orally as 4 placebo tablets once daily in the evening | 1 | 63 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants With Abnormal Hematology Values of PCI-Platelet
- Description
- Number of participants with abnormal Hematology values of PCI were reported. The abnormal values were reported only for platelet, diagnosed at Week 6 or Early withdrawal visit.
- Time frame
- Upto 28-day FU
- Population
- All Subject population
Source ClinicalTrials.gov
Trial
- Title
- A Study of the Effects of a New Antidepressant Treatment (GSK561679) in Females With Major Depressive Disorder
- NCT number
- NCT00733980
- Phases
- PHASE2
- Conditions
- Depressive Disorder, Major
- Interventions
- GSK561679, Placebo
- Lead sponsor
- GlaxoSmithKline
- Results first posted
- 2017-11-17
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00733980?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.govNone 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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