Last updated: February 11, 2025
Sponsor: University Hospital, Grenoble
Overall Status: Completed
Phase
N/A
Condition
Vomiting
Liver Disorders
Hepatic Encephalopathy
Treatment
N/AClinical Study ID
NCT06248736
CHU Grenoble/ ALPACA
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
> 18 years
Patients treated with Lactulose with balloon rectal probe
Exclusion
Exclusion Criteria:
Patient(s) objecting to the use of their data for research purposes
Rectal probe contraindication: damage to the rectal mucosa, rectal surgery, severehaemorrhoids, rectal stenosis, rectal tumour,
Lactulose contraindication (person unable to absorb galactose)
Patients deprived of liberty, under guardianship or curators
Pregnant women
Patient not affiliated to a social security scheme
Study Design
Total Participants: 25
Study Start date:
June 07, 2022
Estimated Completion Date:
August 27, 2024
Connect with a study center
Pr PIERRE BOUZAT
Grenoble, 38000
FranceSite Not Available
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