A RANDOMIZED, CONTROLLED, MULTICENTER PHASE 2 STUDY TO EVALUATETHE EFFICACY AND SAFETY OF FIBRIN SEALANT VH S/D 500 S-APR(TISSEEL) FORHEMOSTASIS IN SUBJECTS UNDERGOING HEPATIC RESECTION - FS VH S/D 500 S-APR IN HEPATIC RESECTIO

Baxter Innovations GmbH0 个研究点开始时间: 2010年7月2日最近更新: 2012年3月19日

适应症

试验速览

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•Preoperative inclusion criteria:
•Signed informed consent obtained from the subject before any study-related activities
•Subject’s age is 18 years or above
•Subject will undergo planned, elective resection of at least 1 anatomical segment of the liver for
•any reason by laparotomy
•Subject is willing and able to comply with the requirements of the protocol
•Female subjects of childbearing potential must present with a negative serum or urine pregnancy
•test within 72 hours before the elective liver resection
•Female subjects of childbearing potential must agree to employ adequate birth control measures
•for the duration of their participation in the study
•Intraoperative inclusion criteria (before randomization):
•Resection of at least 1 anatomical segment of the liver has been performed
•Oozing from the cut surface of the liver persists after conventional resection
•procedure and primary control of arterial and venous bleeding by sutures,
•ligations, clips, vascular stapler, point electrocautery or focal radiofrequency
•Need for additional supportive hemostatic treatment to stop bleeding (i.e.
•diffuse oozing) of the liver resection area
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range

•Preoperative exclusion criteria:
•Subject needs emergency liver surgery
•Subject will undergo liver resection via laparoscopic procedure
•Subject has known congenital coagulation disorder (e.g. hemophilia)
•Subject has known hypersensitivity to any ingredient of the investigational medicinal product
•Suspected inability or unwillingness of the subject to comply with trial procedures
•If female, subject is pregnant or lactating at the time of study enrollment
•Subject has already participated in this study (each subject can only be enrolled once)
•Subject has participated in another clinical study involving an IP or investigational device within
•30 days prior to study enrollment or is scheduled to participate in another clinical study
•involving an IP or investigational device during the course of this study
•Intraoperative Exclusion Criteria (before randomization):
•Occurrence of any severe surgical complication that require resuscitation or
•deviation from the planned surgical procedure.
•Disseminated intravascular coagulopathy (DIC)
•Application of any topical hemostatic material on the resection surface of the
•liver prior to application of the study treatment
•Radiofrequency precoagulation of the liver resection surface, except focal use
•of radiofrequency as primary hemostatic treatment

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