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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03133962
Other study ID # PI2014_843_0013
Secondary ID
Status Withdrawn
Phase N/A
First received April 25, 2017
Last updated May 11, 2017
Start date November 3, 2014
Est. completion date April 21, 2017

Study information

Verified date May 2017
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date April 21, 2017
Est. primary completion date April 21, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Good positioning of the distal end of the catheter by ETT, without repositioning following the scopy 1 day
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