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Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: a Randomized Cohort Study (HEPACOLL)

Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: a Randomized Cohort Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01874639
Enrollment
140
Registered
2013-06-11
Start date
2013-06-30
Completion date
2016-12-31
Last updated
2016-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatectomy

Keywords

Hepatectomy, blood loss, hemostasis, coagulation, Liver surgery (benign or malign), Resection of 2 or more segments

Brief summary

Blood loss in hepatic surgery is the main factor of postoperative morbidity. The use of the most effective possible tool for hemostasis allows a bleeding decrease during liver transection and thus could reduce postoperative morbidity. In the past decade, the improvement of techniques of transection of the hepatic parenchyma was one of the most important factors to ensure the hepatectomy safety. But the clinical performances of these technological innovations (ultrasound dissectors, monopolar radiofrequency probes and dissection devices using pressurized water) remain still unclear. The medical device of hemostasis Aquamantys® (Salient company, Innopath) use the technology of transcollation combining a source of radiofrequency associated with a conductive liquid (NaCl 0.9% solution). The system consists of a specific generator (Aquamantys Pump Generator®) and single-use probes (Aquamantys 2.3 BipolarSealer®). The energy of radiofrequency is delivered by two bipolar electrodes. The innovative aspect of this device consists in maintaining the tissue to a temperature of 100°C, while using a conductive liquid which acts as process of cooling and avoids the drying out of tissues, smoke, risks of electric arc and overheating met with conventional electrosurgery. This device allows the coagulation of blood vessels but also bile ducts. The Aquamantys® system could decrease the postoperative morbidity and mortality due to a decrease of blood loss and biliary leak. These clinical benefits could be translated by an improvement of the direct and indirect costs associated to the surgery. However the Aquamantys® technology has not been scientifically validated in the context of the hepatic surgery, and this technology is expensive due to the purchase of single-use bipolar probes (Aquamantys 2.3 BipolarSealer®) and to the investment in a generator (Aquamantys Pump Generator®). Consequently, it is essential to realize a study measuring the clinical and medical economic impact of the transcollation technology (Aquamantys® device) in the hepatic surgery.

Detailed description

After validation of the inclusion and exclusion criteria, the patients include in this clinical trial will be randomized between the two arms of the study: * Control group: hepatectomy with conventional hemostasis using standard bipolar coagulation * Test group: hepatectomy with Aquamantys®

Interventions

DEVICEstandard bipolar coagulation
DEVICEAquamantys® probe for liver hemostasis

Sponsors

INNOPATH
CollaboratorUNKNOWN
MEDTRONIC labs provide the aquamantys® probes for the study.
CollaboratorUNKNOWN
University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing elective surgery for liver resection of malignant or benign disease * Hepatic resection of two or more segments * No coagulation disorder * No portal hypertension (platelets ≥ 100 G/L, absence of splenomegaly, absence of portal hypertension varices) * Obtaining the patient's written consent

Exclusion criteria

* Age \< 18 years and \> 80 years * ASA score \> 3 * Cirrhosis, liver fibrosis \> F2, steatosis \> 60%, sinusoidal obstruction syndrome * Cognitive troubles and major disability making impossible to understand the study and signed the informed consent (e.g. dementia, psychiatric disorders like psychosis, speech disorder ...) * Liver and kidney failure * Pregnancy and lactating women * Legal incapacity * Patients already enrolled in a clinical trial

Design outcomes

Primary

MeasureTime frame
Blood loss during surgeryat day 0

Secondary

MeasureTime frame
Duration of surgeryat day 0
Duration of hospital stayat day 1
Number of red blood cells transfusionsat day 0
Duration of liver transectionat day 0
Volume of crystalloid and colloid fluidsat day 0
Need of norepinephrine during the surgeryat day 0
Number of frozen plasma transfusionsat day 0

Countries

France

Contacts

Primary ContactPatrick LACARIN
placarin@chu-clermontferrand.fr04 73 75 11 95

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026