Comparison · NCT00550459-2ee8d104
Tolvaptan (15-60 mg) vs Placebo: Number of Patients With Serum Chemistry Laboratory Abnormalities: Glucose
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. Tolvaptan (15-60 mg) vs Placebo: Number of Patients With Serum Chemistry Laboratory Abnormalities: Glucose. Trial comparisons, record NCT00550459-2ee8d104. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00550459-2ee8d104
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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 | 0.117 | wilson | |
| Risk in group 2 | 0.0714 | 0.0198 | 0.226 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0714 | -0.226 | 0.0564 | 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 Tolvaptan (15-60 mg) than on Placebo | 14 | 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 | Tolvaptan (15-60 mg) | Tolvaptan tablet 15-60 mg given once daily for 21 days | 0 | 29 | OG001 |
| Group 2 | Placebo | Placebo tablet given once daily for 21 days | 2 | 28 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Patients With Serum Chemistry Laboratory Abnormalities: Glucose
- Description
- Incidence of potentially clinically significant glucose levels post-baseline (normal range=70-125 mg/dL)
- Time frame
- 28 days
- Population
- Safety population defined as all randomized subjects who consumed at least 1 dose of trial medication
Source ClinicalTrials.gov
Trial
- Title
- Effects of Titrated Oral Tolvaptan 15-60 mg Once Daily (QD) on Cognitive and Neurological Function in Elderly Hyponatremic Patients
- NCT number
- NCT00550459
- Phases
- PHASE3
- Conditions
- Hyponatremia
- Interventions
- Tolvaptan, Placebo
- Lead sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc.
- Results first posted
- 2011-04-28
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00550459?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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