Clinical Trials Directory

Trials / Completed

CompletedNCT03137745

Coagulation Profile of Patients Undergoing CRS(Cytoreductive Surgery) and Hyperthermic Intraperitoneal Chemotherapy

To Study the Changes in Coagulation Profile in Patients Undergoing CRS(CYTOREDUCTIVE SURGERY) and HIPEC(HYPERTHERMIC INTRAPERITONEAL CHEMOTHERAPY)

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
Rajiv Gandhi Cancer Institute & Research Center, India · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

To study the changes in coagulation profile in patients undergoing cytoreductive surgery and Hyperthermic intraperitoneal chemotherapy. The objective of the study is to determine the utility of thromboelastography in comparison to standard coagulation tests in assessing the coagulopathy in patients undergoing CRS with HIPEC.

Detailed description

This is a prospective observational study conducted in 60 patients undergoing CRS with HIPEC in RGCIRC from march 2015- march2016 after taking permission from the institutional review board and informed written consent from the patients. Arterial blood samples were collected before and after HIPEC and on first and second postoperative day for PT,APTT INR,TEG and ABG. Statistical analysis was done using chi square test and unpaired t- test for categorical and continuous variables. Pearson's correlation coefficient was calculated for analysing the correlation between the variables .P - value \<0.05 was considered statistically significant.

Conditions

Interventions

TypeNameDescription
OTHERthromboelastographythromboelastography was done pre HIPEC ,post HIPEC and first and second postoperative days

Timeline

Start date
2015-03-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2017-05-03
Last updated
2017-05-05

Source: ClinicalTrials.gov record NCT03137745. Inclusion in this directory is not an endorsement.