EchoPAC: Evaluation of the Contribution of the Ultrasound Tracking and the Positioning of the Distal End During the Implantation of Implantable Chamber or Long-lasting Venous Catheter

Sponsor
Centre Hospitalier Universitaire, Amiens (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03133962
Collaborator
(none)
0
1
1
29.6
0

Study Details

Study Description

Brief Summary

Given the increase in the number of PAC implants or long-term catheters, and the ease of access to cardiac ultrasound in the operating theaters, the investigator thought to use ultrasound to PAC or long-term catheters.

The investigator considers cardiac echocardiography through its costal pathway to locate the correct positioning of the distal end of the catheter in a manner equivalent to the scopic locating with all the side effects of the irradiation and with Equivalent efficiency

Condition or Disease Intervention/Treatment Phase
  • Other: Adult patients who are candidates for a CAP or long-term central catheter placement
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Evaluation of the Contribution of the Ultrasound Tracking and the Positioning of the Distal End During the Implantation of Implantable Chamber or Long-lasting Venous Catheter
Actual Study Start Date :
Nov 3, 2014
Actual Primary Completion Date :
Apr 21, 2017
Actual Study Completion Date :
Apr 21, 2017

Arms and Interventions

Arm Intervention/Treatment
Other: Patients applying for CAP or long-term central catheter

Other: Adult patients who are candidates for a CAP or long-term central catheter placement
Evaluate the feasibility of finding the correct positioning of the distal end of the PAC or of the long-term catheter by cardiac ultrasound in comparison with the brightness scopy, reference method.

Outcome Measures

Primary Outcome Measures

  1. Good positioning of the distal end of the catheter by ETT, without repositioning following the scopy [1 day]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All adult patients are candidates for a long-term CAP or central catheter placement.

  • Benefiting from sedation or general anesthesia.

Exclusion Criteria:
  • Patient aged <18 years.

  • Pregnant woman.

  • Lack of anesthesiologist with knowledge of ultrasound.

  • Site of femoral puncture

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Amiens Picardie Amiens Picardie France 80054

Sponsors and Collaborators

  • Centre Hospitalier Universitaire, Amiens

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire, Amiens
ClinicalTrials.gov Identifier:
NCT03133962
Other Study ID Numbers:
  • PI2014_843_0013
First Posted:
Apr 28, 2017
Last Update Posted:
May 12, 2017
Last Verified:
May 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of May 12, 2017