search
Back to results

Impact of Weight Loss in Cirrhosis With Obesity and MAFLD (WELCOME)

Primary Purpose

Liver Cirrhosis, Obesity

Status
Recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Weight loss
Sponsored by
Institute of Liver and Biliary Sciences, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Cirrhosis focused on measuring Obesity, liver disease, nutrition, weight loss, fibrosis.

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients between 18 and 65 years.
  • Obese cirrhotics of any etiology.
  • BMI > 30

Exclusion Criteria:

  • Patients with oChild B (8,9) and C oMELD>20

    • High-risk varices
    • HPS/ pleural effusion
    • Alcoholic Hepatitis
    • Chronic Kidney Disease, cardiac, neurological diseases
    • HCC
    • Pregnancy
    • Unwilling patients

Sites / Locations

  • Institute of Liver and Biliary SciencesRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention Arm

Arm Description

In addition to standard pharmacological treatment this group would receive diet comprising of 20-25 kcal and 1.2gm protein per kg ideal body weight per day. The total distribution of the calories would be as 55-60% from carbohydrates, 25% from protein, and 20% from fat. The diet would be explained to the patient with the help of individual diet charts.

Outcomes

Primary Outcome Measures

Number of Patients with change in liver fibrosis with 10% weight loss in 3 months in an obese patient with CLD.

Secondary Outcome Measures

Effect of weight loss (10%) in three months on Insulin resistance (HOMA- IR)
Insulin resistance will be measured at baseline and at 3 months
Effect of weight loss (10%) in three months on Triglyceride levels
Triglyceride levels will be measured at baseline and at 3 months
Effect of weight loss (10%) in three months on blood sugar levels as a component of metabolic syndrome
Blood sugar levels will be noted at baseline and at 3 months
Effect of weight loss (10%) in three months on central obesity as a component of metabolic syndrome
Central obesity will be noted at baseline and at 3 months
Effect of weight loss (10%) in three months on high density lipoprotein (HDL) as a component of metabolic syndrome
High density lipoprotein (HDL)metabolic syndrome will be noted at baseline and at 3 months
Effect of weight loss (10%) in three months on metabolic syndrome
Components of metabolic syndrome will be noted at baseline and at 3 months
Effect of weight loss (10%) in three months on body composition- bio electrical impedance
Body composition by bioelectrical impedance will be measured at baseline and at the end of three months
Effect of weight loss (10%) in three months on anthropometric mid arm muscle circumference (MAMC)
Mid amr muscle circumference (MAMC) will be measured at baseline and at the end of three months
Effect of weight loss (10%) in three months on anthropometric Mid upper arm circumference (MUAC)
Mid upper arm circumference (MUAC) will be measured at baseline and at the end of three months
Effect of weight loss (10%) in three months on anthropocentric tricep fold thickness (TSF)
Tricep fold thickness (TSF) will be measured at baseline and at the end of three months
Effect of weight loss (10%) in three months on functional capacity
Functional capacity will be measured by hand grip dyanamometer at baseline and at the end of three months
Effect of weight loss (10%) in three months on Pro inflammatory marker- (Tumor Necrosis Factor) TNF-alpha
Pro inflammatory marker will be noted at baseline and at 3 months
Effect of weight loss (10%) in three months on Pro inflammatory marker -IL-6
Pro inflammatory marker will be noted at baseline and at 3 months
Effect of weight loss (10%) in three months on Anti inflammatory marker -Adiponectin
Anti inflammatory marker (Adiponectin) will be noted at baseline and at 3 months

Full Information

First Posted
October 3, 2021
Last Updated
February 28, 2023
Sponsor
Institute of Liver and Biliary Sciences, India
search

1. Study Identification

Unique Protocol Identification Number
NCT05104541
Brief Title
Impact of Weight Loss in Cirrhosis With Obesity and MAFLD
Acronym
WELCOME
Official Title
Impact of Weight Loss on Liver Fibrosis in Obese Patients With Cirrhosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 10, 2021 (Actual)
Primary Completion Date
November 9, 2023 (Anticipated)
Study Completion Date
November 9, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute of Liver and Biliary Sciences, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Nutrition therapy is the cornerstone of medical therapy in patients with cirrhosis. 70% compensated patients with Chronic Liver Disease (CLD) are overweight or obese. Obesity in CLD augments decompensation, plausibly through increase in portal pressure. Moreover, the cardiometabolic risk factors are increased with increase in body weight, obesity also has an impact on the already compromised health-related quality of life of patients with CLD. Most feasible, safe, and widely used method of management of obesity is life-style modifications. Hypocaloric with normal to high protein diet along with moderate-intensity exercises have been practiced for weight reduction. These kinds of dietary changes reduce body weight and may bring about favourable changes in the body composition (reduce the body fat percentage but at the same time preserving the lean body mass). Weight loss in obese patients with CLD would in turn improve the clinical outcome, reduce the hepatic complications, moreover weight loss may also improve health related quality of life, and other prognostic markers of the disease like fibroscan along with improvement in the associated metabolic derangements in patients with CLD. There is no Indian data in this context. Thus, through this trial, investigator would be able to ascertain an appropriate lifestyle-related non- intervention regimen that helps in the management of obesity in patients with cirrhosis. Not only that the baseline information of these obese patients with CLD would give us an idea or the profile of the body composition in terms of muscularity, adiposity, sarcopenic obesity (if any), of these patients with CLD.
Detailed Description
Liver disease is one of the main causes of hospital admissions worldwide and the 12th leading cause of mortality in many countries. Among all etiologies (toxic-metabolites, viral, autoimmune, and genetic disorders), nonalcoholic fatty liver disease (NAFLD) features as the most common cause, with increasing prevalence attributed to the epidemic of metabolic syndrome. According to the World Health Organization, in 2014, more than 30% of the United States population were obese and more than 60% overweight. Furthermore, 15% of all Western population and 35% of patients with obesity will develop steatohepatitis (NASH). Hence world over obesity is on a rise, the prevalence of obesity has consistently risen since past four decades in both genders. Indian similar scenario is seen not only in the urban but also in the rural population. This pandemic disease is attributed to both the increased amounts of processed foods high in fructose, sodium, and saturated fats, and the increasingly sedentary lifestyle. Obesity is considered a chronic state of low-grade inflammation, being associated with complications such as metabolic syndrome, type 2 diabetes, hypertension, and cardiovascular disease. It has also been linked with increased risks of certain cancers, such as colon, breast, breast, endometrium, kidney, esophagus, stomach, pancreas, and gallbladder. The combination of obesity, insulin resistance, and NASH is also thought to increase the risk of Hepatocellular Carcinoma (HCC). Most of all obesity in cirrhotics accelerates decompensation plausibly through an increase in portal hypertension. The risk of first clinical decompensation of cirrhosis is approximately three times higher in obese cirrhotics compared to those with normal weight. There are innumerable randomized controlled trials examining the role of various kinds of weight-loss diets and regimens in NAFLD patients, namely Mediterranean diets, Ornish diets, south beach diets, Atkins diets, Zone diet, weight watcher's diets, etc. However, once cirrhosis sets in or is diagnosed the concept of malnutrition akin to undernutrition is the prime consideration in a patient which baffles the physicians. The nutritional guidelines either European Society of Parenteral and Enteral Nutrition (ESPEN) or American Society of Parenteral and Enteral Nutrition (ASPEN) have always focused on a high calorie and a high protein diet in cirrhosis. These guidelines have not even touched upon the topic of obesity in cirrhosis. Moreover, for decades, investigator have been obsessed with the idea of protein restriction in patients with cirrhosis. In the recent past, our attention is drawn towards the other end of the spectrum of malnutrition i.e. obesity, which has been steadily on the rise world over and cirrhotics are no exception. Obesity is associated with poor survival, severe hepatic decompensation, poor post-transplantation outcomes as well as greater difficulty in liver transplantation, and also higher non-response to antiviral therapy in patients with cirrhosis. Hence weight reduction is the standard of care in such patients. A few studies have examined the role of a monitored exercise program including resistance training including cycle ergometric exercises have been shown to favorably change the body composition but none have been done in obese cirrhotics with the aim of weight loss. At the same time, low-calorie and even very-low-calorie ketogenic diets have been tried in obese cirrhosis and published as case series. Based on the magnitude of the problem of obesity in CLD and its detrimental impact on the clinical outcome investigator propose to assess the impact of weight loss with low calorie, high protein diet and moderate physical activity (lifestyle modifications- a non-pharmacological strategy) on liver fibrosis, body composition changes, functional capacity, clinical outcome in obese cirrhotics in this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis, Obesity
Keywords
Obesity, liver disease, nutrition, weight loss, fibrosis.

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective Study
Masking
None (Open Label)
Allocation
N/A
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Arm
Arm Type
Experimental
Arm Description
In addition to standard pharmacological treatment this group would receive diet comprising of 20-25 kcal and 1.2gm protein per kg ideal body weight per day. The total distribution of the calories would be as 55-60% from carbohydrates, 25% from protein, and 20% from fat. The diet would be explained to the patient with the help of individual diet charts.
Intervention Type
Other
Intervention Name(s)
Weight loss
Intervention Description
In addition to standard pharmacological treatment this group would receive diet comprising of 20-25 kcal and 1.2gm protein per kg ideal body weight per day. The total distribution of the calories would be as 55-60% from carbohydrates, 25% from protein and 20% from fat. The diet would be explained to the patient with the help of individual diet charts.
Primary Outcome Measure Information:
Title
Number of Patients with change in liver fibrosis with 10% weight loss in 3 months in an obese patient with CLD.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Effect of weight loss (10%) in three months on Insulin resistance (HOMA- IR)
Description
Insulin resistance will be measured at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on Triglyceride levels
Description
Triglyceride levels will be measured at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on blood sugar levels as a component of metabolic syndrome
Description
Blood sugar levels will be noted at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on central obesity as a component of metabolic syndrome
Description
Central obesity will be noted at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on high density lipoprotein (HDL) as a component of metabolic syndrome
Description
High density lipoprotein (HDL)metabolic syndrome will be noted at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on metabolic syndrome
Description
Components of metabolic syndrome will be noted at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on body composition- bio electrical impedance
Description
Body composition by bioelectrical impedance will be measured at baseline and at the end of three months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on anthropometric mid arm muscle circumference (MAMC)
Description
Mid amr muscle circumference (MAMC) will be measured at baseline and at the end of three months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on anthropometric Mid upper arm circumference (MUAC)
Description
Mid upper arm circumference (MUAC) will be measured at baseline and at the end of three months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on anthropocentric tricep fold thickness (TSF)
Description
Tricep fold thickness (TSF) will be measured at baseline and at the end of three months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on functional capacity
Description
Functional capacity will be measured by hand grip dyanamometer at baseline and at the end of three months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on Pro inflammatory marker- (Tumor Necrosis Factor) TNF-alpha
Description
Pro inflammatory marker will be noted at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on Pro inflammatory marker -IL-6
Description
Pro inflammatory marker will be noted at baseline and at 3 months
Time Frame
3 months
Title
Effect of weight loss (10%) in three months on Anti inflammatory marker -Adiponectin
Description
Anti inflammatory marker (Adiponectin) will be noted at baseline and at 3 months
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients between 18 and 65 years. Obese cirrhotics of any etiology. BMI > 30 Exclusion Criteria: Patients with oChild B (8,9) and C oMELD>20 High-risk varices HPS/ pleural effusion Alcoholic Hepatitis Chronic Kidney Disease, cardiac, neurological diseases HCC Pregnancy Unwilling patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr. Shiv Kumar Sarin, MD, DM, FNA
Phone
011-46300000
Email
shivsarin@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Harshita Tripathi, M.Sc., PDCC
Phone
011-46300000
Email
tripathiharshita0521@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Shiv Kumar Sarin, MD, DM, FNA
Organizational Affiliation
Institute of Liver and Biliary Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Liver and Biliary Sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110070
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr. Shiv Kumar Sarin, MD, DM, FNA
Phone
011-46300000
Email
shivsarin@gmail.com
First Name & Middle Initial & Last Name & Degree
Dr. Shiv Kumar Sarin, MD, DM, FNA
First Name & Middle Initial & Last Name & Degree
Dr. Y.K Joshi, MD, PhD
First Name & Middle Initial & Last Name & Degree
Harshita Tripathi, M.Sc., PDCC

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Impact of Weight Loss in Cirrhosis With Obesity and MAFLD

We'll reach out to this number within 24 hrs