Critical Illness Clinical Trial
Official title:
The Effects of Anti-infective Central Venous Catheter(CVC) on Catheter-related Bloodstream Infection(CRBSI) in Critical Care Patients: a Multiple-center, Randomized, Control Study
The purpose of this study is to investigate the effect of anti-infective central venous catheter(Certofix®Protect) on reducing catheter-related bloodstream infection in critically ill patients in China, and the relationship between catheter-related bloodstream infection and catheter-related thrombosis.
Status | Recruiting |
Enrollment | 1818 |
Est. completion date | December 2018 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - adult patients in intensive care unit (ICU)(age = 18 years) - needs double lumen CVC more than 5 days - Signed informed consent Exclusion Criteria: - thrombosis in target and/or contralateral vein - pregnancy or lactating women - unlikely to survive for more than 1 month - bad prognosis - suspected catheter-related infection - replacement CVC in original site through guide wire - severe burn - situation that is not suitable for CVC, including allergic to CVC material, thrombosis in target vein, infection of puncture site, coagulation disorder, abnormal anatomy - already in this study - participated in other studies within 3 months |
Country | Name | City | State |
---|---|---|---|
China | Peking Union Medical College Hospital | Beijing | Beijing |
China | West China Hospital, Sichuan University | Chengdu | Sichuan |
Lead Sponsor | Collaborator |
---|---|
West China Hospital | Peking Union Medical College Hospital |
China,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | catheter-related bloodstream infection | number of participants with catheter-related bloodstream infection | through study completion, an average of 2 years | |
Secondary | catheter-related thrombosis | number of participants with catheter-related thrombosis | through study completion, an average of 2 years | |
Secondary | all cause mortality | through study completion, an average of 2 years |
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