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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04173910
Other study ID # LPECarotide
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 15, 2020
Est. completion date August 1, 2020

Study information

Verified date October 2020
Source University of Liege
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Verify in ultrasound the impact of a Sellick and LPEC manoeuvre in terms of compression of the carotid artery and decrease in vascular flow.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 1, 2020
Est. primary completion date July 15, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Adults Volunteers

Exclusion Criteria:

- pregnant women

- people with carotid artery defects

- people with an anomaly in the oropharyngeal massif

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ultrasound LPEC/Sellick
We will perform an ultrasound of the carotid artery and then apply a Sellick manoeuvre and a left paratracheal compression of the cervical esophagus respectively.

Locations

Country Name City State
Belgium Javillier Liège

Sponsors (1)

Lead Sponsor Collaborator
University of Liege

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compression of the carotid artery during an esophageal compression manoeuvre Measurement of the diameter of the carotid artery in cross-section and longitudinal section through study completion, an average of 1 month
Primary Vascular flow of the carotid artery during an esophageal compression manoeuvre Measurement of systolic velocities in pulsed Doppler in the carotid artery through study completion, an average of 1 month
Secondary Measurement of the force to be applied to compress the esophagus without compressing the carotid artery use of a dynamometer to measure the force required to exert at the left paratracheal level through study completion, an average of 1 month
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