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CompletedPhase 4

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

The Influence of Appetite-Related Central and Gut Hormones in Modulating Binge Eating Behaviour in Obese and Overweight Healthy Subjects

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

42

actual

Study population

Feeding And Eating Disorders, Obesity / overweight

Key I/E criterion

BMI 30-45

Primary endpoint

Binge eating scale score

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT01739049
Org study IDFF0192012

Timeline

Milestones

Study first posted2012-11-30estimated
Last update posted2017-05-04actual
Study start2012-11 (month precision)
Primary completion2013-10actual (month precision)
Study completion2015-01actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Feeding And Eating DisordersObesity / overweight

Eligibility

Who can enroll

Minimum age18 Years
Maximum age65 Years
SexAll
Healthy volunteersAccepted

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

Endpoints (3)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Weight & body composition
1
Other clinical outcomes
1
Other (unclassified)
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Reduction in weight

Time frame:12 weeks

change from baseline, improvement

Other clinical outcomes

1 endpoint
Primary/protocol endpoint

Reduction in binge eating scale score

Time frame:12 weeks

change from baseline, improvement

Other (unclassified)

1 endpoint
Other/protocol endpoint/low confidence

Profile of hormones

Time frame:12 weeks

descriptive

Publications (1)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.