Overview

Comparison Trial for Chloraprep Versus Aqueous Chlorhexidine (2%) for the Prevention of Catheter-related Bacteremia

Status:
Withdrawn
Trial end date:
2021-04-01
Target enrollment:
0
Participant gender:
All
Summary
A multicentre, open-label clinical trial of two groups comparing cutaneous asepsis with chlorhexidine gluconate at 2% + isopropyl alcohol 70% in relation to the placement of central venous catheters (Study group) with standard asepsis with aqueous chlorhexidine at 2% (Group Control). The incidence of catheter related bacteremia, the incidence of colonization of the skin and the incidence of colonization of the central venous catheter will be evaluated.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Instituto de Investigacion Sanitaria La Fe
Treatments:
Chlorhexidine
Chlorhexidine gluconate
Criteria
Inclusion Criteria:

- Patients admitted to the ICU.

- Patients with age greater than or equal to 18 years.

- Patients who require at least one central venous catheters during 48h or more.

- Obtaining informed consent.

Exclusion Criteria:

- Intolerance or known allergy to chlorhexidine, isopropyl alcohol or orange yellow S
(E110).

- High probability of death within 48 hours after admission.

- Use of coated catheter.

- Previously included in the study.