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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05214079
Other study ID # Strenght_LPP
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date September 1, 2022

Study information

Verified date January 2022
Source University of Liege
Contact Benjamin Javillier, MD
Phone 43667180
Email javillier.benjamin@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Determine the force required to occlude the esophagus with a left paratracheal pressure


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date September 1, 2022
Est. primary completion date July 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Physical status score 1 or 2 - No contre indication to Left Paratracheal pressure Exclusion Criteria: - Obese patients - Physical status score 3, 4 or 5 - Contre indication to Left Paratracheal pressure

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Left paratracheal pressure
Applying Left Paratracheal pressure and testing its effectiveness using gastric tube . in addition , by using the dynamometer , the CP 50 is defined.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Liege

Outcome

Type Measure Description Time frame Safety issue
Primary Necessary force of Left paratracheal pressure to occlude the esophagus in female versus male . an up and down method will define the CP 50 in each gender. A comparison between CP50 in both sex will define exactly our outcome 24 hours
See also
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