CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 248 enrolled
Drug / intervention
Argipressin +1 moredrug
Likely dose
Argipressin 0.056 mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05293041
NCT05293041Phase 4Completed

Influence of Argipressin on Blood Loss During Hepatic Resection; a Double-blinded, Randomized Placebo-controlled Trial (ARG-01)

Kristina Svennerholm·interventional·Posted Mar 24, 2022·Updated Mar 6, 2025

In Brief

A Phase 4 clinical trial evaluating Argipressin and Placebo for Colon Cancer Liver Metastasis and 2 related conditions. Completed, enrolled 248 participants across 1 site.

Detailed Summary

Infusion of Argipressin during hepatic resection surgery may reduce blood loss. It may also reduce transfusion requirements, and mitigate the perioperative inflammatory response compared to placebo. Subjects will be randomized to infusion of Argipressin or placebo during surgery. Blood loss, transfusion requirements, surgical data including length of stay in hsopital, inflammatory markers and markers of renal- intestinal- and cardiac injury will be assessed. Two sub-studies has been added; one for evaluation of coagulation function, and one for assessment of pain scores and morphine consumption.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSweden
Collaborators--

Timeline

Phase 4CompletedFinished
2023202420252026
First PostedMar 24, 2022
Enrollment StartMar 27, 2022
Primary CompletionDec 6, 2024
Study CompletionFeb 17, 2025
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 4.3 years ago

Interventions

Argipressindrug

Infusion of Argipressin 0.8 U/ml, 0.056 ml/kg/h will be started as soon as the central line is placed, and continued until the end of surgery in the treatment arm.

Placebodrug

Infusion of Normal Saline 0.056 ml/kg/h will be started as soon as the central line is placed, and continued until the end of surgery in the placebo arm.