Trial · NCT02368249
Does Terlipressin Improve Renal Outcome After Liver Surgery
NCT02368249, Phase 2, Withdrawn, University of Zurich
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Does Terlipressin Improve Renal Outcome After Liver Surgery. Trials, record NCT02368249. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02368249
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Does Terlipressin Improve Renal Outcome After Liver Surgery
- NCT number
- NCT02368249
- Status
- Withdrawn
- Phases
- Phase 2
- Enrollment
- 0 participants, actual
- Lead sponsor
- University of Zurich
- Conditions
- Kidney Failure
- Interventions
- Terlipressin, Placebo
- First posted
- 2015-02-23
- Last updated
- 2017-05-05
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | serum creatinine peak level within 48 hours post-operative | within 48 hours post-operative | |
| Secondary | the urinary output/24h | Post Operative Day 0 to 3 | |
| Secondary | Need for hemofiltration and/or hemodialysis | Post Operative Day 0 - 14 | participants will be followed for the duration of hospital stay, an expected average of 14 days |
| Secondary | Morbidity & mortality | Post Operative Day 0 - 14 | measured by the comprehensive complication index; participants will be followed for the duration of hospital stay, an expected average of 14 days |
| Secondary | Liver function | Post Operative Day 0 - 5 | assessed by serum levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) |
| Secondary | length of hospital stay | Post Operative Day 0 - 14 | in days; participants will be followed for the duration of hospital stay, an expected average of 14 days |
| Secondary | length of ICU stay | Post Operative Day 0 - 7 | in days; participants will be followed for the duration of ICU stay, an expected average of 7 days |
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/NCT02368249
GET https://conductscience.org/api/trials/v1/NCT02368249/registered