Evaluation of the Occurrence of Acute Complications Caused by a Central Venous Catheter Placement

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1780 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-11-30

Study Completion Date

2013-03-31

Brief Summary

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It is an observational, prospective, monocentric study. The purpose of the study is to assess the acute complications rate caused by a central venous catheter placement.

All the patients who require a central venous placement could be enrolled in the study.

The study will not change the usual practice. The placement will be on day 1 and patients will be contacted by phone on day 7 to identify potential complications and to assess pain.

Anaesthesia staff will keep patients under surveillance to control the absence of late complications.

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Detailed Description

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Conditions

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Anesthesia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Central venous catheter

All patients who require the placement of a central venous catheter

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Age \>= 18.
* Patient who requires the placement of a central venous catheter (a portacath (PAC), a peripherally inserted central catheter (PICC) or a tunnelled catheter).
* Patient able to understand, read and write French.
* Mandatory affiliation with a health insurance system.

Exclusion Criteria

* Active infection at placement of the central venous catheter.
* Patient who can't be contacted by phone.
* Patient who is likely to have a femoral venous catheter placement.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No