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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04856826
Other study ID # 38RC19.419
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 5, 2021
Est. completion date June 1, 2026

Study information

Verified date December 2023
Source University Hospital, Grenoble
Contact Julie Duhoo
Phone +33476767094
Email jduhoo@chu-grenoble.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare the number of attempts to place a peripheral venous catheter in the group of patients hospitalized in the post-emergency unit and benefiting from echo guidance and therapeutic communication, to the group of patients hospitalized on the post-emergency unit using traditional technique.


Recruitment information / eligibility

Status Recruiting
Enrollment 276
Est. completion date June 1, 2026
Est. primary completion date May 10, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Hospitalized in the post-emergency unit - Requiring the placement of a venous catheter in the post-emergency unit - Affiliation to social security or benefiting from such a scheme - Informed and written consent signed Exclusion Criteria: - Protected person (art. L1121-5 to L1121-8 of the CSP) - Patient included in another interventional study - Patient already included for a first catheter placement in the post-emergency unit.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ultrasound guidance and therapeutic communication
insertion of a peripheral venous catheter with ultrasound guidance and therapeutic communication

Locations

Country Name City State
France CHU Grenoble Alpes La Tronche

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary successful placement of a venous catheter on the first attempt percentage of successful placement of a venous catheter on the first attempt within the hour after insertion of peripheral venous catheter
Secondary patient experience not validated Satisfaction questionnaire and pain scale. score between 0 and 30 corresponding to high satisfaction within the hour after insertion of peripheral venous catheter
Secondary number of attempts to insert a peripheral venous catheter Average in each group of the number of attempts within the hour during insertion of peripheral venous catheter
Secondary number of calls for a second nurse in the service Average in each group of the number of service's interveners for a catheter placement within the hour during insertion of peripheral venous catheter
Secondary number of calls to a nurse anesthetist Average in each group of the number of external interveners within the hour during insertion of peripheral venous catheter
Secondary location of the final placement site Proportion of patients in each group according to the location of the final placement site within the hour during insertion of peripheral venous catheter
Secondary the caliber of the catheter placed Proportion of patients in each group according to the caliber of the catheter placed within the hour during insertion of peripheral venous catheter
Secondary infectious or thromboembolic events total number of infectious or thromboembolic events at the implantation site during the patient's stay in the post-emergency unit 4 days
Secondary duration of catheter placement Average duration, in minutes, of catheter placement in each group within the hour during insertion of peripheral venous catheter
Secondary functional life of the catheter functional life of the catheter, by group. 4 days
Secondary Satisfaction of nursing staff not validated Satisfaction questionnaire for nursing staff in the post-emergency unit . score between 0 and 55 corresponding to a high satisfaction at the end of study inclusion, at 6 month
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