Perioperative coagulation abnormalities in patients undergoing HIPEC surgery
Not Applicable
- Conditions
- Health Condition 1: C569- Malignant neoplasm of unspecifiedovary
- Registration Number
- CTRI/2023/10/058904
- Lead Sponsor
- Malabar cancer centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients undergoing CRS and HIPEC
patients >18 years and <80 years
Exclusion Criteria
patients undergoing CRS not proceeding for HIPEC
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To find out the incidence of perioperative coagulopathyTimepoint: preoperative and first five postoperative days
- Secondary Outcome Measures
Name Time Method to find out the factors affecting perioperative coagulopathy & to find out the incidence of postoperative thromboembolic complicationsTimepoint: 4 weeks