Trial · NCT02009878
Results by group63
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 63
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Maximal Increase From Baseline in Serum Sodium Concentration Following Tolvaptan Administration. | Tolvaptan 3.75 mg | 3.6 | Standard Deviation 3.3 | mmol/L | |
| Maximal Increase From Baseline in Serum Sodium Concentration Following Tolvaptan Administration. | Tolvaptan 7.5 mg | 5.3 | Standard Deviation 2.5 | mmol/L | |
| Maximal Increase From Baseline in Serum Sodium Concentration Following Tolvaptan Administration. | Tolvaptan 15 mg | 7.9 | Standard Deviation 5.3 | mmol/L | |
| Cmax (Maximum (Peak) Plasma Concentration) for Tolvaptan in Plasma. | Tolvaptan 3.75 mg | 37.7 | Standard Deviation 12.6 | ng/mL | |
| Cmax (Maximum (Peak) Plasma Concentration) for Tolvaptan in Plasma. | Tolvaptan 7.5 mg | 107 | Standard Deviation 48.9 | ng/mL | |
| Cmax (Maximum (Peak) Plasma Concentration) for Tolvaptan in Plasma. | Tolvaptan 15 mg | 157 | Standard Deviation 68.1 | ng/mL | |
| Tmax (Time to Maximum (Peak) Plasma Concentration) for Tolvaptan in Plasma | Tolvaptan 3.75 mg | 1.50 | Full Range 0.95 to 4.00 | hours | |
| Tmax (Time to Maximum (Peak) Plasma Concentration) for Tolvaptan in Plasma | Tolvaptan 7.5 mg | 2.00 | Full Range 1.00 to 4.00 | hours | |
| Tmax (Time to Maximum (Peak) Plasma Concentration) for Tolvaptan in Plasma | Tolvaptan 15 mg | 2.00 | Full Range 0.97 to 3.00 | hours | |
| AUC Infinity (Area Under the Concentration-time Curve From Time Zero to Infinity) for Tolvaptan in Plasma | Tolvaptan 3.75 mg | 244 | Standard Deviation 90.7 | ng·h/mL | |
| AUC Infinity (Area Under the Concentration-time Curve From Time Zero to Infinity) for Tolvaptan in Plasma | Tolvaptan 7.5 mg | 655 | Standard Deviation 373 | ng·h/mL | |
| AUC Infinity (Area Under the Concentration-time Curve From Time Zero to Infinity) for Tolvaptan in Plasma | Tolvaptan 15 mg | 1000 | Standard Deviation 361 | ng·h/mL | |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 3.75 mg | (Day 0) 12 hour (N= 10, 9, 9) | -2.5 | Standard Deviation 1.3 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 7.5 mg | (Day 0) 12 hour (N= 10, 9, 9) | -2.3 | Standard Deviation 3.0 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 15 mg | (Day 0) 12 hour (N= 10, 9, 9) | -2.6 | Standard Deviation 2.2 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 3.75 mg | (Day 1) 2 hour (N= 10, 10, 8) | -2.0 | Standard Deviation 4.4 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 7.5 mg | (Day 1) 2 hour (N= 10, 10, 8) | 2.4 | Standard Deviation 1.3 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 15 mg | (Day 1) 2 hour (N= 10, 10, 8) | 1.7 | Standard Deviation 1.8 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 3.75 mg | (Day 1) 4 hour (N= 10, 10, 8) | -1.7 | Standard Deviation 4.7 | mmol/L |
| Change From Baseline in Serum Sodium Concentrations | Tolvaptan 7.5 mg | (Day 1) 4 hour (N= 10, 10, 8) | 3.5 | Standard Deviation 3.0 | mmol/L |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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GET https://conductscience.org/api/trials/v1/NCT02009878/results