← Trials/Trial dossier/NCT02616003

CompletedPhase 4

Preoperative Condition in Giant Obese Patients

A Novel Preoperative Conditioning Therapy in Giant Obese Patients With the Combination of Liraglutide and a Leucine-Based Amino-Acid Infusion and Caloric Restriction

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

50

actual

Study population

Bariatric Surgery Candidate, Obesity / overweight

Key I/E criterion

Primary endpoint

Operability

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 IDNCT02616003
Org study IDFF 121/2015

Timeline

Milestones

Study first posted2015-11-26estimated
Last update posted2021-03-23actual
Study start2014-04actual (month precision)
Primary completion2018-01actual (month precision)
Study completion2018-04actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Bariatric Surgery CandidateObesity / overweight

Eligibility

Who can enroll

SexAll
Healthy volunteersNot accepted

Inclusion criteria

multimorbid, super-super obese patients

Exclusion criteria

renal insufficiency III

Endpoints (10)

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

MASH / liver
2
Cardiometabolic biomarkers
2
Other clinical outcomes
2
Other (unclassified)
2
Weight & body composition
1
Glycemic / diabetes
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Preoperative excess weight loss in %

Time frame:21 days

percent change from baseline, improvement

Glycemic / diabetes

1 endpoint
Secondary/protocol endpoint

Hg A1c in %

Time frame:21 days

descriptive, improvement

LOINC 4548-4

MASH / liver

2 endpoints
Secondary/protocol endpoint

Liver volume

Time frame:21 days

change from baseline, improvement

Secondary/protocol endpoint

Liver function

Time frame:21 days

change from baseline, improvement

Cardiometabolic biomarkers

2 endpoints
Secondary/protocol endpoint

Chronic inflammation

Time frame:21 days

hs-CRP, change

change from baseline, improvement

LOINC 30522-7

Secondary/protocol endpoint

Chronic inflammation II

Time frame:21 days

change from baseline, improvement

Other clinical outcomes

2 endpoints
Primary/protocol endpoint

Operability

Time frame:21 days

categorical status, improvement

Secondary/protocol endpoint

Pulmonary function

Time frame:21 days

change from baseline, improvement

Other (unclassified)

2 endpoints
Secondary/protocol endpoint/low confidence

Total Protein in g/l

Time frame:21 days

descriptive

Secondary/protocol endpoint/low confidence

Albumin in g/l

Time frame:21 days

descriptive

Publications (7)

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.