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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06109584
Other study ID # 02-23-270-088
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date August 2024

Study information

Verified date October 2023
Source Consorci Sanitari de Terrassa
Contact Paula Gil Esteller, MD
Phone +34 628467708
Email gilesteller@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators propose a prospective diagnostic validity study in which the correct location of the central venous catheter will be verified by ultrasound and then verified by radiography in the same patient, without modifying the usual clinical practice criteria.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date August 2024
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients over 18 years of age in whom a decision is made to place a supradiaphragmatic central venous catheter. - Patients who agree to participate in the study Exclusion Criteria: - Patients with devices that may interfere with the ultrasound images. - Patients with poor ultrasound window - Patients with superior vena cava syndrome

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Insertion of central venous catheter
Central venous catheter verified by ultrasound and then verified by radiography.

Locations

Country Name City State
Spain Consorci Sanitari de Terrassa Terrassa Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Consorci Sanitari de Terrassa

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine the incidence of malposition of central venous catheter Incidence of malposition measured by echocardiography and chest radiography in confirming the correct positioning of the tip of the supradiaphragmatic central venous catheter. Moreover, this check can be performed in a shorter time interval. Through study completion, an average of 1 year
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