← Trials/Trial dossier/NCT02488057

CompletedPhase 4

Improving Beta Cell Function in Mexican American Women With Prediabetes

Assets

GLP-1 / incretin class catch-all / Liraglutide

Listed sites

4

Recruiting sites

Enrollment

360

actual

Study population

Obesity / overweight, Prediabetes / glucose intolerance

Key I/E criteria

BMI 30-42Female

Primary endpoint

Beta Cell Function

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 IDNCT02488057
Org study ID2014H0478

Timeline

Milestones

Study first posted2015-07-02estimated
Last update posted2019-08-28actual
Study start2016-05 (month precision)
Primary completion2019-03actual (month precision)
Study completion2019-03actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweightPrediabetes / glucose intolerance

Eligibility

Who can enroll

Minimum age18 Years
Maximum age40 Years
SexFemale
Healthy volunteersNot accepted

Inclusion criteria

Mexican-american
Female
BMI 30-42
willingness to complete protocol
pre-diabetic
English or Spanish literate

Exclusion criteria

pregnant
30 min or more of moderate to vigorous activity more than 3 times per week
cardiovascular disease
physical limitations that might be aggravated by moderate physical activity
planning to move in next 12-24 months
diabetic

Endpoints (8)

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

Cardiometabolic biomarkers
4
Glycemic / diabetes
2
Weight & body composition
1
Other (unclassified)
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Waist Circumference

Time frame:3 months

Waist circumference, change

change from baseline, improvement

Glycemic / diabetes

2 endpoints
Primary/protocol endpoint/low confidence

Beta Cell Function

Time frame:3 months

change from baseline, improvement

Secondary/protocol endpoint

Fasting Glucose

Time frame:3 months

Fasting glucose, change

change from baseline, improvement

LOINC 1558-6

Cardiometabolic biomarkers

4 endpoints
Secondary/protocol endpoint

Triglycerides

Time frame:3 months

Triglycerides, change

change from baseline, improvement

LOINC 2571-8

Secondary/protocol endpoint

HDL cholesterol

Time frame:3 months

HDL-C, change

change from baseline, improvement

LOINC 2085-9

Secondary/protocol endpoint

Blood Pressure

Time frame:3 months

change from baseline, improvement

Secondary/protocol endpoint

Heart Sensitive C-reactive protein

Time frame:3 months

hs-CRP, change

change from baseline, improvement

LOINC 30522-7

Other (unclassified)

1 endpoint
Secondary/protocol endpoint/low confidence

Presence of genetic polymorphisms

Time frame:3 months

categorical status, descriptive

Publications (10)

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.