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

NCT01405534 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1780

Last updated 2014-09-12

No results posted yet for this study

Summary

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.

Conditions

  • Anesthesia

Sponsors & Collaborators

  • Centre Leon Berard

    lead OTHER

Principal Investigators

  • Hervé ROSAY, MD · Centre Leon Berard

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2013-03-31
Completion
2013-03-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01405534 on ClinicalTrials.gov