Impact of Weight Loss in Cirrhosis With Obesity and MAFLD (WELCOME)
Impact of Weight Loss on Liver Fibrosis in Obese Patients With Cirrhosis
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.
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Dr. Shiv Kumar Sarin, MD, DM, FNA
- Phone Number: 011-46300000
- Email: shivsarin@gmail.com
Study Contact Backup
- Name: Harshita Tripathi, M.Sc., PDCC
- Phone Number: 011-46300000
- Email: tripathiharshita0521@gmail.com
Study Locations
-
-
Delhi
-
New Delhi, Delhi, India, 110070
- Recruiting
- Institute of liver and Biliary Sciences
-
Contact:
- Dr. Shiv Kumar Sarin, MD, DM, FNA
- Phone Number: 011-46300000
- Email: shivsarin@gmail.com
-
Principal Investigator:
- Dr. Shiv Kumar Sarin, MD, DM, FNA
-
Sub-Investigator:
- Dr. Y.K Joshi, MD, PhD
-
Sub-Investigator:
- Harshita Tripathi, M.Sc., PDCC
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Intervention Arm
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. |
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. |
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
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
|
3 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of weight loss (10%) in three months on Insulin resistance (HOMA- IR)
Time Frame: 3 months
|
Insulin resistance will be measured at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on Triglyceride levels
Time Frame: 3 months
|
Triglyceride levels will be measured at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on blood sugar levels as a component of metabolic syndrome
Time Frame: 3 months
|
Blood sugar levels will be noted at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on central obesity as a component of metabolic syndrome
Time Frame: 3 months
|
Central obesity will be noted at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on high density lipoprotein (HDL) as a component of metabolic syndrome
Time Frame: 3 months
|
High density lipoprotein (HDL)metabolic syndrome will be noted at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on metabolic syndrome
Time Frame: 3 months
|
Components of metabolic syndrome will be noted at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on body composition- bio electrical impedance
Time Frame: 3 months
|
Body composition by bioelectrical impedance will be measured at baseline and at the end of three months
|
3 months
|
|
Effect of weight loss (10%) in three months on anthropometric mid arm muscle circumference (MAMC)
Time Frame: 3 months
|
Mid amr muscle circumference (MAMC) will be measured at baseline and at the end of three months
|
3 months
|
|
Effect of weight loss (10%) in three months on anthropometric Mid upper arm circumference (MUAC)
Time Frame: 3 months
|
Mid upper arm circumference (MUAC) will be measured at baseline and at the end of three months
|
3 months
|
|
Effect of weight loss (10%) in three months on anthropocentric tricep fold thickness (TSF)
Time Frame: 3 months
|
Tricep fold thickness (TSF) will be measured at baseline and at the end of three months
|
3 months
|
|
Effect of weight loss (10%) in three months on functional capacity
Time Frame: 3 months
|
Functional capacity will be measured by hand grip dyanamometer at baseline and at the end of three months
|
3 months
|
|
Effect of weight loss (10%) in three months on Pro inflammatory marker- (Tumor Necrosis Factor) TNF-alpha
Time Frame: 3 months
|
Pro inflammatory marker will be noted at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on Pro inflammatory marker -IL-6
Time Frame: 3 months
|
Pro inflammatory marker will be noted at baseline and at 3 months
|
3 months
|
|
Effect of weight loss (10%) in three months on Anti inflammatory marker -Adiponectin
Time Frame: 3 months
|
Anti inflammatory marker (Adiponectin) will be noted at baseline and at 3 months
|
3 months
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Dr. Shiv Kumar Sarin, MD, DM, FNA, Institute of liver and Biliary Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- ILBS-Cirrhosis-45
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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