Trial · NCT02468063
To Assess the Efficacy of Early Introduction of a Combination of Low Dose Vasopressin Analogue in Addition to Noradrenaline as a Vasopressor in Patients of Cirrhosis With Septic Shock
NCT02468063, Not applicable, Completed, Institute of Liver and Biliary Sciences, India
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. To Assess the Efficacy of Early Introduction of a Combination of Low Dose Vasopressin Analogue in Addition to Noradrenaline as a Vasopressor in Patients of Cirrhosis With Septic Shock. Trials, record NCT02468063. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02468063
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- To Assess the Efficacy of Early Introduction of a Combination of Low Dose Vasopressin Analogue in Addition to Noradrenaline as a Vasopressor in Patients of Cirrhosis With Septic Shock
- NCT number
- NCT02468063
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 184 participants, actual
- Lead sponsor
- Institute of Liver and Biliary Sciences, India
- Conditions
- Cirrhosis With Septic Shock
- Interventions
- Low dose terlipressin, Noradrenaline, Noradrenaline
- First posted
- 2015-06-10
- Last updated
- 2017-11-06
Source ClinicalTrials.gov
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Target MAP (Mean Arterial Pressure) >65 mm Hg at 6 hrs | 6 hours | |
| Secondary | Maintenance of target MAP (Mean Arterial Pressure) | 2 days | MAP is Mean Arterial pressure SVR is Sustained Virologic Response |
| Secondary | Survival | 28 days | |
| Secondary | Survival | 48 hours | |
| Secondary | Microcirculation (lactate level, Lactate clearance, SCVO2, ABG-VBG Pco2 difference), | 2 years | |
| Secondary | Tissue perfusion (lactate level, Lactate clearance, SCVO2, ABG-VBG Pco2 difference), | 2 years | |
| Secondary | Effect on - AKI (Acute kidney Injury), | 2 years | |
| Secondary | Effect on variceal bleed | 2 years | |
| Secondary | Effect on rebound hypotension | 2 years | |
| Secondary | Effect on organ failure | 2 years |
1 to 10 of 15Source ClinicalTrials.gov
See all 15 registered outcomesOutcomes0
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/NCT02468063
GET https://conductscience.org/api/trials/v1/NCT02468063/registered