Description of Lactulose Administration by Balloon Rectal Tube in Severe Hepatic Encephalopathy

Last updated: February 11, 2025
Sponsor: University Hospital, Grenoble
Overall Status: Completed

Phase

N/A

Condition

Vomiting

Liver Disorders

Hepatic Encephalopathy

Treatment

N/A

Clinical Study ID

NCT06248736
CHU Grenoble/ ALPACA
  • Ages > 18
  • All Genders

Study Summary

Acute liver failure in cirrhotic patients is associated with a one-month mortality of 48%. Encephalopathy, largely related to hyperammonemia, is a frequent complication of liver failure and is a poor prognostic marker. Lactulose decreases ammonia by acidification of the colon, replacement of urease-producing bacteria and creation of a laxative effect. Thus, the administration of lactulose in patients with severe hepatic encephalopathy reduces mortality by more than 40%.

In intensive care patients, lactulose is often administered rectally. The use of simple rectal tubes is associated with frequent leakage of lactulose as well as faecal discharge and therefore risks of infection and skin lesions. Balloon rectal tubes with a drug delivery valve have recently been developed and used in this indication. The aim of this study is therefore to describe the use of these balloon rectal tubes to administer Lactulose in severe hepatic encephalopathy.

This suggests that ammonia reduction in these patients may prolong survival time.

No studies have described the administration of Lactulose via the rectal route with a balloon tube. The descriptive methodology is therefore appropriate. This is a preliminary study allowing data collection to establish the methodology for a subsequent clinical trial.

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
    France

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.