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Secondary Prophylaxis of Hepatic Encephalopathy in Cirrhotic Patients

Primary Purpose

Hepatic Encephalopathy

Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
lactulose
colistin
Sponsored by
Madonna Magdy Fahmy
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Hepatic Encephalopathy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • • Age >18 years.

    • Patients with liver cirrhosis and previous history of recovery from hepatic encephalopathy.

Exclusion Criteria:

  • • History of taking lactulose in past 7 days

    • Patients on secondary prophylaxis for spontaneous bacterial peritonitis
    • Patients on psychoactive drugs, such as antidepressants or sedatives
    • Previous transjugular intrahepatic portosystemic shunts or shunt surgery
    • Significant comorbid illness such as heart, respiratory, or neurological disease such as Alzheimer's disease and Parkinson's disease
    • Hepatocellular carcinoma or other neoplasias that could shorten life expectancy
    • Recent infection or antibiotic use within last 6 weeks
    • Recent gastrointestinal bleeding in the past 6 weeks
    • Renal insufficiency, myasthenia gravis.
    • Hypersensitivity to colistin sulfate.
    • Pregnancy or lactation
    • Alcohol intake

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    patients that will receive lactulose

    patients that will receive colistin

    Arm Description

    Cirrhotic patients who were recovered from HE will be randomized into lactulose group receiving 30-60 ml of lactulose orally in 2 or 3 divided doses so that patient passed 2-3 semisoft stools per day

    colistin group receiving colistin sulfate 1.5 million I.U. tablet orally twice

    Outcomes

    Primary Outcome Measures

    Development of overt hepatic encephalopathy
    Number of Participants with Development of overt hepatic encephalopathy encephalopathy according to West Haven criteria

    Secondary Outcome Measures

    Health related quality of life
    HRQOL assessment using chronic liver disease questionnaire (higher score equates to worse quality of life)

    Full Information

    First Posted
    February 9, 2022
    Last Updated
    March 6, 2022
    Sponsor
    Madonna Magdy Fahmy
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05279586
    Brief Title
    Secondary Prophylaxis of Hepatic Encephalopathy in Cirrhotic Patients
    Official Title
    Secondary Prophylaxis of Overt Hepatic Encephalopathy in Cirrhosis: a Randomized Controlled Trial of Colistin Versus Lactulose
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    March 2022 (Anticipated)
    Primary Completion Date
    February 2023 (Anticipated)
    Study Completion Date
    March 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Madonna Magdy Fahmy

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    The aim of this study is to compare the efficacy and safety of colistin versus lactulose for secondary prophylaxis of overt hepatic encephalopathy in patients with liver cirrhosis.
    Detailed Description
    Hepatic encephalopathy (HE) is a reversible neuropsychiatric changes, it occurs in 30%-45% of cirrhotic patients during their life. Once HE is developed, the 1-year mortality exceeds 60%. The high morbidity and mortality combined with the costs underline the importance of effective treatment and prevention of HE. The exact pathogenesis of HE is still unknown but ammonia is known to play a key role. Strategies to prevent and treat HE aims at reducing the production and absorption of gut derived neurotoxins, particularly ammonia, mainly through bowel cleansing, non absorbable disaccharides and non -absorbable antibiotics. Patients with previous episode of overt HE, have a 40% cumulative risk of recurrence at 1 year. Because recurrent episodes of HE are associated with increased health care burden, poor prognosis, and risk of death, prevention of the recurrence of HE should be considered in each patient. After an episode of overt HE has resolved, patients with cirrhosis should receive secondary prophylactic therapy for an indefinite period of time or until they undergo liver transplantation. Lactulose is considered the first line for secondary prophylaxis of overt HE while rifaximin is add-on therapy to lactulose. Non-absorbable disaccharides like lactulose acts as both osmotic laxative, and gut acidifying agent reducing the production and the absorption of ammonia from the intestines by changing the gut microbiota. However, side effects of lactulose therapy including excessively sweet taste and gastrointestinal side effects such as abdominal pain, bloating, flatulence, severe and unpredictable diarrhea possibly leading to dehydration result in frequent non-adherence in clinical practice. Lactulose non-adherence, reported as a factor in 39% of hospital admissions, was the single most frequent precipitant of overt HE . Rifaximin is a non-absorbable antibiotic with low systemic absorption, broad antimicrobial spectrum, and low frequency of side effects. It has a place in prevention of recurrence of HE when lactulose alone fails. However, the accessibility of rifaximin may be limited by its high cost. Colistin sulfate is a polymyxin antibiotic which is active against aerobic gram-negative bacteria including most enterobacteria except Proteus. It is poorly absorbed from the gastrointestinal tract. Colistin sulfate being not systemically absorbed is used orally for bowel decontamination and treatment of intestinal infections. Oral colistin is used for peri-operative selective decontamination of digestive tract in elective colorectal cancer patients in combination with tobramycin and amphotericin B. Also, combining oral colistin with ciprofloxacin has been effective in the prevention of Gram-negative sepsis in neutropenic patients without the emergence of significant resistance. However, no study up till now focuses on the use of oral colistin in the secondary prophylaxis of hepatic encephalopathy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hepatic Encephalopathy

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    316 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    patients that will receive lactulose
    Arm Type
    Active Comparator
    Arm Description
    Cirrhotic patients who were recovered from HE will be randomized into lactulose group receiving 30-60 ml of lactulose orally in 2 or 3 divided doses so that patient passed 2-3 semisoft stools per day
    Arm Title
    patients that will receive colistin
    Arm Type
    Active Comparator
    Arm Description
    colistin group receiving colistin sulfate 1.5 million I.U. tablet orally twice
    Intervention Type
    Drug
    Intervention Name(s)
    lactulose
    Other Intervention Name(s)
    duphlac
    Intervention Description
    all interventions are used in secondary prophylaxis in cirrhotic patients
    Intervention Type
    Drug
    Intervention Name(s)
    colistin
    Intervention Description
    all interventions are used in secondary prophylaxis in cirrhotic patients
    Primary Outcome Measure Information:
    Title
    Development of overt hepatic encephalopathy
    Description
    Number of Participants with Development of overt hepatic encephalopathy encephalopathy according to West Haven criteria
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    Health related quality of life
    Description
    HRQOL assessment using chronic liver disease questionnaire (higher score equates to worse quality of life)
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: • Age >18 years. Patients with liver cirrhosis and previous history of recovery from hepatic encephalopathy. Exclusion Criteria: • History of taking lactulose in past 7 days Patients on secondary prophylaxis for spontaneous bacterial peritonitis Patients on psychoactive drugs, such as antidepressants or sedatives Previous transjugular intrahepatic portosystemic shunts or shunt surgery Significant comorbid illness such as heart, respiratory, or neurological disease such as Alzheimer's disease and Parkinson's disease Hepatocellular carcinoma or other neoplasias that could shorten life expectancy Recent infection or antibiotic use within last 6 weeks Recent gastrointestinal bleeding in the past 6 weeks Renal insufficiency, myasthenia gravis. Hypersensitivity to colistin sulfate. Pregnancy or lactation Alcohol intake
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Madonna Magdy Fahmy, Master
    Phone
    01099794496
    Email
    madona.magdy@med.tanta.edu.eg
    First Name & Middle Initial & Last Name or Official Title & Degree
    Lobna Ahmed Abo Ali, professor
    Phone
    01147117052
    Email
    lobna_fahmy@yahoo.com

    12. IPD Sharing Statement

    Learn more about this trial

    Secondary Prophylaxis of Hepatic Encephalopathy in Cirrhotic Patients

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