← Trials/Trial dossier/NCT02616003
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
Lead sponsor
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
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
Exclusion criteria
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
Weight & body composition
1 endpointPreoperative excess weight loss in %
Time frame:21 days
percent change from baseline, improvement
Glycemic / diabetes
1 endpointHg A1c in %
Time frame:21 days
descriptive, improvement
LOINC 4548-4
MASH / liver
2 endpointsLiver volume
Time frame:21 days
change from baseline, improvement
Liver function
Time frame:21 days
change from baseline, improvement
Cardiometabolic biomarkers
2 endpointsChronic inflammation
Time frame:21 days
hs-CRP, change
change from baseline, improvement
LOINC 30522-7
Chronic inflammation II
Time frame:21 days
change from baseline, improvement
Other clinical outcomes
2 endpointsOperability
Time frame:21 days
categorical status, improvement
Pulmonary function
Time frame:21 days
change from baseline, improvement
Other (unclassified)
2 endpointsTotal Protein in g/l
Time frame:21 days
descriptive
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
- Clinical nutrition ESPEN2022 Aug (month)PMID35871930doi:10.1016/j.clnesp.2022.05.009via clinicaltrials gov reference derived + pubmed nct search
- The New England journal of medicine2015 Jul 2PMID26132939doi:10.1056/NEJMoa1411892via CT.gov reference
- The Journal of clinical investigation2014 Oct (month)PMID25202976doi:10.1172/JCI78371via CT.gov reference
- Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014 Aug (month)PMID24681814doi:10.1038/npp.2014.74via CT.gov reference
- Journal of physiology and biochemistry2013 Mar (month)PMID22535285doi:10.1007/s13105-012-0170-2via CT.gov reference
Provenance
Sources
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.