Trial · NCT01386372
Tolvaptan for In-hospital Hyponatremia
NCT01386372, Phase 2, Terminated, Mario Negri Institute for Pharmacological Research
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Tolvaptan for In-hospital Hyponatremia. Trials, record NCT01386372. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01386372
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Tolvaptan for In-hospital Hyponatremia
- NCT number
- NCT01386372
- Status
- Terminated
- Phases
- Phase 2
- Enrollment
- 3 participants, actual
- Lead sponsor
- Mario Negri Institute for Pharmacological Research
- Conditions
- Hyponatremia
- Interventions
- Tolvaptan, Standard therapy
- First posted
- 2011-07-01
- Last updated
- 2016-12-15
- Other registries' IDs
- eudract:2010-024431-17
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Changes from baseline in proportion of subjects with normonatremia at 6 month. | At 1,2,3,4 and 10 day, and at 1,2,4 and 6 month.. | |
| Primary | Changes from baseline in serum sodium levels from basal at 6 months. | At 1,2,3,4, 10 day and at 1,2,4 and 6 month.. | |
| Secondary | Proportion of subjects achieving normonatremia at discharge and at predefined time-points. | 8 hours, 1, 2, 3, and 10 days and 1, 2, 4 and 6 months after randomization | |
| Secondary | Absolute changes in serum sodium levels vs baseline at predefined time-points. | 8 hours, 1, 2, 3, and 10 days and 1, 2, 4 and 6 months after randomization |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01386372
GET https://conductscience.org/api/trials/v1/NCT01386372/registered