A clinical study to compare the effectiveness and safety of intermittent flushing of central venous catheters with heparin ,normal saline in adults to prevent occlusion.
Not Applicable
Recruiting
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2021/04/033007
- Lead Sponsor
- SRM Medical College Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with size 7fr Triple lumen catheter
-Duration of catheter placed up to 14 days
Exclusion Criteria
•Pregnancy
•Allergic to heparin
•Patient refusal
•Coagulation disorders
•Hemodialysis catheter
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occlusion of Central venous cathetersTimepoint: 14 days
- Secondary Outcome Measures
Name Time Method compare lumen patencyTimepoint: checked daily for 14 days <br/ ><br>
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie catheter occlusion in ICU patients with central venous catheters?
How does heparin compare to normal saline in maintaining CVC patency in ICU patients with sepsis?
Are there specific biomarkers that predict catheter-related thrombosis risk in critically ill adults?
What are the potential adverse events associated with heparin flushing in ICU patients with coagulopathy?
What combination therapies or alternative anticoagulants show promise for CVC occlusion prevention in SRM Medical College Hospital studies?