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Clinical Trials/NCT02025894
NCT02025894
Completed
Not Applicable

Risk Factors for Thromboembolic and Infectious Complications Related to Percutaneous Central Venous Catheters in Cancer - Prospective Multicenter Study

Institut de Cancérologie de la Loire27 sites in 1 country3,032 target enrollmentJune 2010
ConditionsCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
Institut de Cancérologie de la Loire
Enrollment
3032
Locations
27
Primary Endpoint
Thromboembolic complications:
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to identify risk factors for thromboembolic and /or infectious complications in 3,000 patients with solid tumor and receiving a Percutaneous Central Venous Catheter (PCVC). A better understanding of the risk factors for these complications in this population would then allow interventional studies to be proposed to assess the benefit of prophylactic procedures in a sub-group of patients at most risk.

Registry
clinicaltrials.gov
Start Date
June 2010
End Date
March 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Institut de Cancérologie de la Loire
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient with a neoplastic solid tumour with an indication for insertion of a PCVC.

Exclusion Criteria

  • Haematological neoplasm pathology, PCVC removal scheduled within 2 weeks of insertion,
  • Therapeutic doses of anticoagulants required at inclusion,
  • PCVC inserted by the femoral vein

Outcomes

Primary Outcomes

Thromboembolic complications:

Time Frame: one year

Locoregional or disseminated infectious complications:

Time Frame: one year

Secondary Outcomes

  • Medical and economic consequences of these complications(one year)

Study Sites (27)

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