Clinical Trials Directory

Trials / Completed

CompletedNCT01957852

FloSeal in CRS and HIPEC

Can FloSeal Reduce the Risk of Intra-abdominal Bleeding After Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy Performed for the Treatment of Peritoneal Carcinomatosis ?

Status
Completed
Phase
Study type
Observational
Enrollment
86 (actual)
Sponsor
Maisonneuve-Rosemont Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Introduction Modern treatment of peritoneal carcinomatosis (PC) combines an aggressive cytoreductive surgery (CRS) of all macroscopic disease and hyperthermic intraperitoneal chemotherapy (HIPEC) performed at the time of surgery. It is considered a high risk procedure and post-operative intra-abdominal bleeding is a major issue as it can delay recovery and promote intra-abdominal infections. In most severe cases (10 to 20% of patients), a second surgery to control the bleeding will be necessary. Major causes of bleeding are : radical resection, extensive peritonectomy, length of surgery, massive transfusion and use of HIPEC. To reduce the risk of intra-abdominal hemorrhage, many strategies have been tried and one of these is the liberal use of FloSeal, but there is no data in this particular field of interest. Over the last 18 months, the investigators have started to use FloSeal in all their cases with large PC and they have observed a dramatic reduction in the rate of reoperation for bleeding and probably secondarily, in the use of blood products, but this has not been measured. Hypothesis FloSeal can reduce the risk of bleeding after CRS and HIPEC procedure. Primary objective To evaluate if the use of FloSeal can reduce the risk of reoperation after CRS and HIPEC procedure in the treatment of PC. Secondary objectives * To evaluate if the use of FloSeal can reduce operative blood loss. * To evaluate if the use of FloSeal can reduce the need of blood products after CRS and HIPEC procedure. * To evaluate if the use of FloSeal can have an impact on other common surgical complications (which can be indirectly bleeding related). * To evaluate if the use of FloSeal can have an impact on length of hospital stay.

Conditions

Interventions

TypeNameDescription
OTHERFloSeal

Timeline

Start date
2008-01-01
Primary completion
2013-03-01
Completion
2013-04-01
First posted
2013-10-08
Last updated
2015-02-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01957852. Inclusion in this directory is not an endorsement.