Trial · NCT07111221
Portal Inflow Modulation Prior to Liver Transplantation in Patients With Increased Risk of Intraoperative Blood Loss
NCT07111221, Not applicable, Recruiting, Medical University of Warsaw
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Portal Inflow Modulation Prior to Liver Transplantation in Patients With Increased Risk of Intraoperative Blood Loss. Trials, record NCT07111221. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07111221
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Portal Inflow Modulation Prior to Liver Transplantation in Patients With Increased Risk of Intraoperative Blood Loss
- NCT number
- NCT07111221
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 104 participants, estimated
- Lead sponsor
- Medical University of Warsaw
- Conditions
- Liver Cirrhosis, Clinically Significant Portal Hypertension
- Interventions
- Transjugular Intrahepatic Portosystemic Shunt, Non-selective beta-blockers
- First posted
- 2025-08-08
- Last updated
- 2025-08-08
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of red blood cell units transfused during liver transplantation. | Intraoperative | |
| Secondary | Portal vein blood flow | Intraoperative | Blood flow velocity in the portal vein during liver transplantation |
| Secondary | Intraoperative blood loss | Intraoperative | Blood loss during liver transplantation \[ml\] |
| Secondary | Operation time | Intraoperative | Time of surgery \[min\] |
| Secondary | Postoperative complications | Up to 90 days | CCI index and the percentage of complications ≥ grade 3 according to the Clavien-Dindo classification after liver transplantation |
| Secondary | Time of hospitalisation | Up to 90 days | Postoperative hospitalisation \[days\] |
| Secondary | Variceal bleeding | Preoperative | Esophageal variceal bleeding before transplantation |
| Secondary | Overall survival | Up to 90 days | Survival from the time of qualification for liver transplantation and up to 90 days after liver transplantation |
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/NCT07111221
GET https://conductscience.org/api/trials/v1/NCT07111221/registered