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Clinical Trials/NCT01638702
NCT01638702
Completed
Not Applicable

Assessment of Impact of Choice of Arm for Access on Rate of Complications in Peripherally Inserted Central Venous Catheters

Richard Lindsay2 sites in 1 country203 target enrollmentOctober 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bacterial Infections
Sponsor
Richard Lindsay
Enrollment
203
Locations
2
Primary Endpoint
Line infection rate
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Peripherally inserted central catheter (PICC) are catheters that are placed mainly in the arms, but which pass in the veins to beside the heart. They are associated with occasional complications due to infection or blockage of the vein that they are in. The investigators want to investigate whether PICCs in the right arm have lower complications than those in the left. This difference in complication rates has been noticed in most other forms of central venous access.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
September 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Richard Lindsay
Responsible Party
Sponsor Investigator
Principal Investigator

Richard Lindsay

MD

McGill University Health Centre/Research Institute of the McGill University Health Centre

Eligibility Criteria

Inclusion Criteria

  • Referral for in-patient PICC placement at centre carrying out study.

Exclusion Criteria

  • Out of hospital referrals for PICC placement; previous PICC placement; previous long term central catheter/pacemaker; unable to give valid consent; presence of pre-existing medical preventing randomisation.

Outcomes

Primary Outcomes

Line infection rate

Time Frame: From insertion to line removal, an estimated time of 4 weeks

All patients will be followed from the point of time of randomisation and PICC insertion until the line develops a complication or is removed. The average length of duration of line access in our institution is 4 weeks.

Secondary Outcomes

  • Effect of number of lumens(From insertion to time of removal, an estimated average time of four weeks.)

Study Sites (2)

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