Influence of Appetite Related Hormones in Binge Eating Behaviour Among the Overweight and Obese

NCT ID: NCT01739049

Last Updated: 2017-05-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-11-30

Study Completion Date

2015-01-31

Brief Summary

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Malaysia has increasing challenges in lifestyle related diseases, which is related to eating habits and disorders. According to the National Health \& Morbidity Survey in 2011; it was reported the prevalence of obesity is 15.1% in 2011; or 2.5 million of the population,; an increase of 7/9% when compared to the 14% prevalence in 2006. Binge eating is a symptom described in various eating disorders. It is an under-diagnosed medical condition closely linked to higher body mass index (BMI) or obesity as well as personality psychopathology, psychiatric and psychological disturbances. Meta-analysis has demonstrated that extremely strict restriction in dietary calorie and fat intake is needed to achieve meaningful weight loss. Appetite and satiety are influenced by extremely complex central and gut-related hormonal systems which modulate the regulation of food intake Centrally acting hormones include Neuropeptide Y (NPY), agouti gene-related peptide, orexin which are appetite-stimulating, melanocortins and alpha-melanocortin-stimulating hormone which promote satiety.

Gut-related peptides include ghrelin secreted by the stomach and the duodenum has orexigenic (appetite stimulating) effect; leptin secreted by adipose tissue has anorexic (appetite inhibiting) effect, cholecystokinin, glucagon-like peptide-1 (GLP-1) secreted by the proximal gastrointestinal tract which has slight anorexic effect, and peptide YY (PYY).

Appetite and obesity have also been commonly related to stress and may influence binge-eating episodes. Previous studies have demonstrated that high stress hormone cortisol is associated with increased appetite and cravings, with preference for high carbohydrate content, thus leading to weight gain.

In the previous study performed by our group on 738 normal subjects who were staffs of the Ministry of Health, Putrajaya, we found a prevalence of 19% binge eating behaviour, 83% of whom were either obese or overweight.

GLP-1 analogue used for the treatment of type 2 diabetes and is also shown to produce and maintain weight loss. Liraglutide, which provides a supra physiological amount of GLP-1 may cause appetite inhibition thus may benefit in reducing binge eating. The aim of this study is to closely observe the extensive profile of neuropeptide Y, ghrelin, leptin and GLP-1, influenced by a standard meal in binge eaters in comparison to non-binge eating controls. In addition, we aim to determine the association between binging and the respective appetite-related hormones and also cortisol. Finally we will also be assessing the efficacy of novel hormonal treatment of Liraglutide in reducing binge eating.

Detailed Description

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Conditions

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Binge Eating Behaviour

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Liraglutide and lifestyle counselling

Liraglutide 0.6mg od for 1st week, then 1.2mg od for 2nd week then 1.8mg od until 12 weeks.

Diet and Exercise

Group Type EXPERIMENTAL

Liraglutide

Intervention Type DRUG

liraglutide

Diet and Exercise

Intervention Type BEHAVIORAL

diet and exercise

Lifestyle counselling

Diet and Exercise

Group Type ACTIVE_COMPARATOR

Diet and Exercise

Intervention Type BEHAVIORAL

diet and exercise

Interventions

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Liraglutide

liraglutide

Intervention Type DRUG

Diet and Exercise

diet and exercise

Intervention Type BEHAVIORAL

Other Intervention Names

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Victoza

Eligibility Criteria

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Inclusion Criteria

* Subjects who are willing to participate and sign informed consent form
* Subjects who are able to answer the questionnaire
* Subjects who are between 18-65 years old
* Subjects with BMI 30-45
* Subjects who are willing to administer injection

Exclusion Criteria

* Pregnant subjects
* Subjects with chronic medical illness such as end stage renal failure, hepatic failure, diabetes mellitus, thyroidism, etc
* Subjects on medication that may influence appetite, satiety and weight
* Subjects that plan to move out of state/country
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universiti Kebangsaan Malaysia Medical Centre

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nor Azmi Kamaruddin, Professor of Medicine

Role: PRINCIPAL_INVESTIGATOR

UKMMC

Rohana Abdul Ghani, Ass Professor of Medicine

Role: PRINCIPAL_INVESTIGATOR

UKMMC

Suehazlyn Zainuddin, MMed

Role: PRINCIPAL_INVESTIGATOR

UKMMC

Wan Nazaimoon Wan Mohamud, Phd Biochemistry

Role: PRINCIPAL_INVESTIGATOR

IMR

Sarah Anne Robert, Mpharm

Role: PRINCIPAL_INVESTIGATOR

UKMMC

Locations

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University Kebangsaan Malaysia Medical Centre

Kuala Lumpur, Kuala Lumpur, Malaysia

Site Status

Countries

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Malaysia

References

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Robert SA, Rohana AG, Shah SA, Chinna K, Wan Mohamud WN, Kamaruddin NA. Improvement in binge eating in non-diabetic obese individuals after 3 months of treatment with liraglutide - A pilot study. Obes Res Clin Pract. 2015 May-Jun;9(3):301-4. doi: 10.1016/j.orcp.2015.03.005. Epub 2015 Apr 11.

Reference Type DERIVED
PMID: 25870084 (View on PubMed)

Other Identifiers

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FF0192012

Identifier Type: -

Identifier Source: org_study_id

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