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Trial · Interventional

Status unknownPhase 3Registry data

Comparing Effects of Liraglutide and Bariatric Surgery on Weight Loss, Liver Function, Body Composition, Insulin Resistance, Endothelial Function and Biomarkers of Non-alcoholic Steatohepatitis (NASH) in Obese Asian Adults

Short name CGH-LiNASH

Overview

Status
Status unknown
Phase
Phase 3
Enrollment
36 participants (estimated)
Sponsor
Changi General Hospital · Other
Design
Not randomized · Open label (no masking)
Countries
1 country

Singapore

Start
Mar 2014
Primary completion
Dec 2017
Completion
Dec 2018 (estimated)
First posted
13 Jan 2016 (estimated)
Last update posted
30 Jan 2018
Conditions
Non-alcoholic Fatty Liver Disease (NAFLD) · Weight Loss · Non-alcoholic Steatohepatitis (NASH)

Timeline

1 trial

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
201420152016201720182019
  1. Ph 3

    CGH-LiNASH

    NCT02654665

    Mar 2014 to est. Dec 2018

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

Non-alcoholic fatty liver disease (NAFLD) is defined by presence of hepatic steatosis (fat accumulation in liver cells), either by imaging or by biopsy and absence of causes for secondary hepatic fat accumulation such as significant alcohol consumption, medications, or hereditary disorders. In the majority of patients, NAFLD is associated with risk factors for cardiovascular disease such as obesity, diabetes mellitus, and high cholesterol, and may lead to irreversible liver damage. Non-alcoholic steatohepatitis (NASH) is a more severe form of NAFLD and is present in up to 30% of obese adults. NASH is defined by hepatic steatosis and inflammation with hepatocyte injury with or without fibrosis (hardening of the liver). The prevalence, morbidity and mortality of NAFLD is increasing, particularly in the Asia-Pacific region where there will be an estimated 300 million obese people by 2030. Weight loss is the first-line treatment for NAFLD in obese individuals, but the utility of lifestyle modification with diet and exercise is limited by difficulties in sustaining compliance and by eventual weight regain. Bariatric (weight loss) surgery produces the greatest amount of weight loss but is limited by cost, patient acceptance, and complications. The efficacy of drugs for NASH, such as vitamin E and medication to lower cholesterol and glucose, remains unclear. Liraglutide, a glucagon-like peptide (GLP-1) analogue, is an injectable medication which has been shown to induce weight loss and lower glucose in obese adults. There is little information on the effects of GLP-1 analogues on NASH, particularly in comparison to other modalities of weight loss such as surgery. This study aims to compare the efficacy and safety of lifestyle modification, liraglutide and surgery, for weight loss in conjunction with reducing severity of NASH, and for insulin resistance, high cholesterol and other cardiovascular risk factors.

Interventions

  • Lifestyle modificationBehavioral
  • LiraglutideDrug

Arms3

  • Experimental

    Liraglutide

    Liraglutide will be administered once daily by subcutaneous injection at a starting dose of 0.6 mg, increasing at 0.6 mg/week increments to a maximum of 3.0 mg over the next 6 weeks, as tolerated.

  • Active comparator

    Bariatric Surgery

    Subjects will have outcomes measured within 28 days before surgery. Post-operative management and frequency of follow-up visits will be decided by the bariatric surgeon. Study visits for biochemical and endothelial function testing; MRI and liver biopsy and / or fibroscan will follow the same schedule as that of the lifestyle and liraglutide arms. Target weight loss for the first 26 weeks post-surgery is at least 30% of excess body weight.

  • Active comparator

    Diet modification and exercise

    Exercise will be used to induce and maintain weight loss in a 26-week Weight Management Program. Each subject will follow an aerobic exercise prescription of moderate intensity (60-75% maximum heart rate) to expend 2000-3000 kcal/week, lasting 30-60 minutes each session (over 5-7 sessions). Subjects will be instructed by sports trainers, compliance reviewed and adjusted if necessary to maintain the targeted total energy expenditure to produce weight loss of at least 7% over 26 weeks.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Improvement in NASH

    Time frame · 12 months

    Registry description

    Reduction/normalization in transaminases, liver fat

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

A trial that is still running, or that stopped early, may post results later.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Randomized controlled trial · 2019

7 results

Randomized trial comparing effects of weight loss by liraglutide with lifestyle modification in non-alcoholic fatty liver disease.

Khoo et al. 2019Liver international : official journal of the International Association for the Study of the Livercited by 110

PMID 30721572DOI 10.1111/liv.14065PUB-30721572

Full text at the publisher7 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 21 Years up to 65 Years
Healthy volunteers
Accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Body mass index \> 27.5 kg/m2 * Waist circumference (WC) \> 90 cm (male) or \> 80 cm (female) * Diagnosis of NASH based on Liver Function Test Results ,Ultrasound Hepato-Biliary System (HBS) findings and / or Liver Biopsy * HbA1c \< 8%\* \*Subjects in the bariatric surgery arm will not need to fulfil this criterion. Exclusion Criteria: * Currently using insulin-sensitising agents (metformin, pioglitazone), weight loss medication (orlistat, phentermine). Patients taking any of these drugs will require a three month washout period before enrolment. * Pregnancy * Significant cardiovascular or respiratory disease * Renal impairment with eGFR \< 60 ml/min * Hepatitis B or C carrier, liver disease other than NAFLD * History of pancreatitis * Personal or family history of multiple endocrine neoplasia type 2 or thyroid carcinoma * Untreated hypothyroidism or hyperthyroidism * Current psychiatric illness * Cardiac pacemaker, metallic prosthetic heart valves and other contraindications to MRI scan * Current smoker * Alcohol intake ≥ 14 units/week

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