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
About this trial
This is an interventional other trial for Hepatic Encephalopathy
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
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
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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