Clinical Trials Directory

Trials / Terminated

TerminatedNCT02728167

Efficacy of HIFU-AR on Blood Loss Reduction in Patients With Liver Metastases Requiring Hepatectomy

Randomized, Open-label, Phase II Study to Evaluate the Efficacy of High-Intensity Focused Ultrasound Assisted Hepatic Resection (HIFU-AR) on Blood Loss Reduction in Patients With Liver Metastases Requiring Hepatectomy

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Centre Leon Berard · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate whether HIFU-assisted liver resection (HIFU-AR) results in reduced blood loss compared to standard liver resection in patients with LM.This is a prospective, monocentric, randomized (1:1 ratio), comparative, open-label Phase II study.

Conditions

Interventions

TypeNameDescription
DEVICEPre-coagulation of the liver parenchyma with HIFU6 to 10 (or more if necessary) side-to-side 40-seconde HIFU treatments

Timeline

Start date
2016-04-01
Primary completion
2018-07-01
Completion
2018-08-01
First posted
2016-04-05
Last updated
2018-08-15

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02728167. Inclusion in this directory is not an endorsement.

Efficacy of HIFU-AR on Blood Loss Reduction in Patients With Liver Metastases Requiring Hepatectomy (NCT02728167) · Clinical Trials Directory