Liver Cirrhoses Clinical Trial
— METALICOfficial title:
Metabolic and Clinical Effects of Enteral Nutrition Therapy: Measured Versus Estimated Energy and Substrate Requirements in Critically Ill Cirrhotics-A Randomized Controlled Trial
Verified date | September 2022 |
Source | Institute of Liver and Biliary Sciences, India |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Part I- Observational study In the first part , investigator would investigate and compare the energy requirements and substrate utilization in healthy subjects and in patients with liver cirrhosis of various etiologies across the disease severity state viz compensated, stable decompensated, critically ill cirrhotics. The investigator would also enroll patients with chronic kidney disease, critically ill patients of acute liver failure or acute on chronic liver failure as disease controls. Part II- Randomized Controlled Study All the eligible, critically ill cirrhotic patients on mechanical ventilator support would be randomized to a control group (receiving the nutritional therapy as per the standard enteral nutritional practice in a critical care setting) or the intervention group (receiving enteral nutrition based on proposed measured requirements by Indirect calorimetry (IC) given till the patient is in ICU(Intensive care unit). The IC would be done thrice a week in both groups.
Status | Completed |
Enrollment | 83 |
Est. completion date | August 31, 2022 |
Est. primary completion date | August 31, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: Disease groups: • Patients with liver cirrhosis (diagnosis established based on routine clinical, biochemical and at least radiological, endoscopic or histological parameters.) admitted in Liver coma Intensive care unit and those admitted in ward. Disease controls: - Patients with Acute liver failure (diagnosis established based on routine clinical, biochemical and at least radiological parameters) admitted in Liver coma Intensive care unit - Patients with severe acute pancreatitis (diagnosis established based on routine clinical, biochemical and at least radiological parameters) admitted in Liver coma Intensive care unit Healthy Controls: - Healthy subjects- Relatives of patients with no known chronic diseases (Chronic obstructive pulmonary disease, Coronary artery disease, Type 2 diabetes, Hypertension, Hypothyroidism, Koch's disease) or not on any long term medications. - Patients with liver cirrhosis (diagnosis established based on routine clinical, biochemical and at least radiological, endoscopic or histological parameters.) admitted in Liver coma Intensive care unit who require mechanical ventilation Exclusion Criteria: - Age<18 years - Active upper gastrointestinal bleeding - If there are conditions which precluded IC, such as an FiO2 >60 %, failure to cooperate, agitation, seizure activity, spasticity, or positive end-expiratory pressure (PEEP) >10 mmHg. - Pregnant women - Refused to consent/ inability to obtain informed consent. - Known long standing diabetic - If there is any evidence of medical/surgical instability - Hepatocellular carcinoma Extrahepatic malignancies - With persistent gastrointestinal dysfunction and ileus - Patients who would be readmitted to the ICU - Known long standing diabetic - Terminally ill patients on high inotropic support - Acute liver failure - If there is any evidence of medical/surgical instability - If patients are taking any portion of nutrition by mouth. - Pregnant women - Refused to consent/ inability to obtain informed consent. - Patient on CRRT- continuous renal replacement therapy - Severe co morbidities such as Chronic kidney disease requiring maintenance dialysis, COPD and Cardiac pathologies (Acute myocardial infarction, heart failure, ). - Hepatocellular carcinoma Extrahepatic malignancies - Moribund patient with likely survival <24 hours - Patients enrolled in other drug trials. |
Country | Name | City | State |
---|---|---|---|
India | ILBS | New Delhi | Delhi |
Lead Sponsor | Collaborator |
---|---|
Institute of Liver and Biliary Sciences, India |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Part 1: An Observational study | Study groups :
Healthy controls Disease Groups Patients with liver cirrhosis (compensated and decompensated) Critically ill cirrhotics on mechanical ventilator support patients with chronic kidney disease (CKD) (stable,non dialyzed, non oliguric outpatients) Critically ill patients with Acute liver failure (ALF) on mechanical ventilator support Critically ill patients with Acute on chronic liver failure(ACLF) on mechanical ventilator support Severe acute pancreatitis on mechanical ventilator support Comparison of the prevalence of hyper and hypo metabolism in patients with chronic liver disease(CLD) and healthy controls and other disease groups. |
One day (Observational) | |
Primary | Part 2: A Randomized controlled trial | Study group:Critically ill Cirrhotic: Diagnosed cases of liver cirrhosis with 2 or more organ failures (liver + renal/circulatory or respiratory failures) requiring ICU admission and on mechanical ventilator support meeting inclusion and exclusion criteria The difference in the duration of mechanical ventilation in critically ill ventilated patients with liver cirrhosis when the nutritional therapy delivered as per estimated energy requirements versus measured requirements | From date of enrollment until the date of ICU discharge /Leaving against medical advice, date of death from any cause, or off ventilatory support whichever comes first, assessed up to 28 days. | |
Secondary | Change in metabolic profile | The effect of nutritional therapy as per estimated energy requirements versus measured requirements in critically ill ventilated patients with liver cirrhosis on the Insulin resistance, ketone bodies, Non-esterified fatty acids (NEFA), amino acids profile and blood sugar levels would be studied | The metabolic parameters would be assessed at the baseline, Day 7 and at Day 15 of enrollment | |
Secondary | Change in inflammatory milieu | The effect of nutritional therapy as per estimated energy requirements versus measured requirements in critically ill ventilated patients with liver cirrhosis on the levels of interleukin 6 (IL-6), Tumor necrosis factor(TNF alfa), CRP(C reactive protein)would be studied | The inflammatory markers would be assessed at the baseline, Day 7 and at Day 15 of enrollment | |
Secondary | Change in clinical parameters | The effect of nutritional therapy as per estimated energy requirements versus measured requirements in critically ill ventilated patients with liver cirrhosis ondevelopment of new onset infection, resolution of sepsis, renal function and length of stay in the ICU/hospital would be studied | The clinical parameters would be assessed daily from the date of enrollment until the date of ICU discharge, date of death from any cause, or out of mechanical ventilatory support whichever comes first, assessed up to 28 days. | |
Secondary | Change in ventilatory and arterial blood gas parameters | The effect of nutritional therapy as per estimated energy requirements versus measured requirements in critically ill ventilated patients with liver cirrhosis on ventilator parameters (FiO2, PEEP, PF ratio) and arterial blood gas parameters( PO2, PCO2, lactate, SpO2) would be studied | The ventilatory and arterial blood gas parameters would be assessed daily from the date of enrollment until the date of ICU discharge, date of death from any cause, or out of mechanical ventilatory support whichever comes first, assessed up to 28 days. | |
Secondary | Change in nutritional parameters | The effect of nutritional therapy as per estimated energy requirements versus measured requirements in critically ill ventilated patients with liver cirrhosis on nutritional parameters( NUTRIC score, feed intolerance and would be studied | The nutritional parameters would be assesses at regular intervals maximum upto 28 days | |
Secondary | The association between energy metabolism, nutritional status and disease severity in patients with CLD | The association between energy metabolism (resting energy expenditure- REE, substrate utilization and macronutrient oxidation), nutritional status (by body composition and anthropometry)and disease severity in patients with CLD (CTP and MELD scores) would be studied | one day (Observational) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT03219372 -
Pravastatin Intervention to Delay Hepatocellular Carcinoma Recurrence
|
Phase 2 | |
Recruiting |
NCT03624517 -
Comparison of 24-hours Versus 72-hours of Octreotide Infusion in Preventing Early Rebleed From Esophageal Varices
|
Phase 4 | |
Recruiting |
NCT04057287 -
Risk Factors of Liver Fibrosis Among First Degree Relatives of Patients With NASH Related Cirrhosis (NRC)
|
||
Recruiting |
NCT04089878 -
"To Study the Impact of Balloon-occluded Retrograde Transvenous Obliteration (BRTO)/Plug Assisted Retrograde Transvenous Obliteration (PARTO) Mediated Portal Flow Modulation in Reduction of Ammonia and Improvement in Organ Volume and Functionality in Patients of Cirrhosis With LR Shunt
|
N/A | |
Completed |
NCT04212286 -
Comparing the Diagnostic Efficiencies of CEUS and EOB-MRI in Patients With High Risk of HCC
|
N/A | |
Completed |
NCT04474743 -
Malnutrition in Chronic Gastrointestinal Diseases, Cross-sectional Study
|
||
Recruiting |
NCT03694691 -
Developing Viability Index for Machine Perfused Livers
|
N/A | |
Terminated |
NCT04072601 -
Statins for Prevention of Disease Progression and Hospitalization in Liver Cirrhosis
|
Phase 4 | |
Terminated |
NCT03878563 -
Alterations in Intestinal Mucosal Barrier Visualized by Confocal Laser Endomicroscopy in Liver Cirrhosis: a Pilot Trial (AMBIC)
|
||
Terminated |
NCT04160039 -
Early Cycle Ergometry for Critically-Ill Liver Failure Patients in a Transplant Intensive Care Unit
|
N/A | |
Recruiting |
NCT04191369 -
EGD vs EUS in Diagnosing Portal Hypertension in Cirrhotic Patients.
|
N/A | |
Completed |
NCT03083925 -
Viatorr CX Case-control Study for Complications of Portal Hypertension
|
||
Not yet recruiting |
NCT03855709 -
Antibiotic-resistant Bacterial Infection of Hepatic Patients
|
||
Recruiting |
NCT02484573 -
Evaluation of Intestinal Permeability in Cirrhotic Patients Before and After Treatment With Non-selective Beta Blocker (Propranolol)
|
N/A | |
Recruiting |
NCT04357600 -
Umbilical Cord Mesenchymal Stem Cell for Liver Cirrhosis Patient Caused by Hepatitis B
|
Phase 1/Phase 2 | |
Completed |
NCT03156426 -
Prognostic Biomarkers For Acute Kidney Injury In Liver Cirrhosis
|
||
Active, not recruiting |
NCT03868397 -
Preoperative Portal and Splanchnic Flow Measurement Using MRI
|
N/A | |
Terminated |
NCT03650660 -
Concordance Between Echocardiographic Assessment Performed in the Initial Phase of Decompensated Cirrhosis With Edema and Ascites by an Expert Intensive Care Physician and a Non-expert Gastroenterologist
|
||
Completed |
NCT03283176 -
Hematologic Profile, Vit. B12 and Folic Acid in Cirrhotics Received Sofosbuvir and Daclatasvir With or Without Ribavirin
|
||
Recruiting |
NCT03172273 -
Early Use of TIPS With Polytetrafluoroethylene(PTFE) Covered Stents in Cirrhotic Patients With Refractory Ascites
|
N/A |