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Delfa

← All trials/NCT02783196

LIR-CG

UnknownPhase NA

Effect of Liraglutide on Clock Genes

Advantages of Liraglutide Mediated Through Its Effect on Clock Gene mRNA Expression

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

-

Estimated enrollment

14

Study population

Type 2 diabetes

Eligibility highlights

BMI 26-32HbA1c 7-10%

Primary endpoint

Clock Gene expression

Registered trial locations

Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT02783196
Org study ID0100-16 WOMC

Timeline

Milestones

Study first posted2016-05-26estimated
Last update posted2016-05-26estimated
Study start2016-07 (month precision)
Primary completion2016-12estimated (month precision)
Study completion2017-06estimated (month precision)

Assets

Investigational agents

Who this study enrolls

Type 2 diabetes

Who can enroll

Minimum age30 Years
Maximum age75 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

1. Patients with T2D diagnosed that were diagnosed < 20 years.

2. HbA1c: 7 to 10 % at screening and at qualification

3. BMI: 26-32 kg/m2.

4. Men and women

5. Between the ages of 30 and 75 years.

6. Patients treated with diet alone or diet plus metformin and SGLT2 inhibitors, at a stable dose for at least 3 months.

7. Concomitant medication i.e. antihypertensive, anti-lipidemic, anti-thrombotic drugs will be allowed.

8. Patients that usually wake up between 06:00 and 07:00 and go to sleep between 22:00 and 24:00.

9. Subjects should not have shift work within 6 month of the study and should not have crossed time zones within 1 month of the study.

10. For woman of child bearing potential, negative pregnancy test and willingness to use birth control during the study :

Exclusion criteria

1. Type 1 diabetes or secondary forms of diabetes.

2. Use of glucose-lowering therapy apart from metformin and SGLT2 inhibitors.

3. Treatment with GLP-1 receptor agonists, dipeptidyl peptidase-4 (DPP-4) inhibitors within the last 3 months.

4. Major illness with life expectancy < 5 years.

5. Serum creatinine level >2mg/d or renal dysfunction: (estimated glomerular filtration rate <45 mL/min/1.73 m2).

6. Hepatic dysfunction: liver disease or transaminase levels >3-fold above normal.

7. History of acute or chronic pancreatitis or high risk for pancreatitis i.e. triglycerides over 400 mg/dl or alcoholism.

8. Family or personal history of Multiple Endocrine Neoplasia type 2 (MEN-2) or familial medullary thyroid carcinoma.

9. Familial or personal history of multiple endocrine neoplasia type 2 (MEN2), familial or non-familial medullary thyroid carcinoma (MTC)

10. Malignant neoplasm requiring chemotherapy, surgery, radiation or palliative therapy within the previous 5 years (with the exception of basal cell skin cancer).

11. Those taking psychotropic, anorectic medication, steroid treatment or with illicit drug abuse or alcoholism within one year prior to study onset.

12. Congestive heart failure and all cardiac arrhythmias i.e. atrial fibrillation.

13. Pregnancy or lactation.

14. Eating disorders and subjects after bariatric surgery or affected by gastroparesis.

15. Night or rotating shift workers or those who crossed more than 2 time zones during the 2-week period prior to study onset.

16. No change in medication or nutrition supplements or physical activity will be made during the study period.

17. Known proliferative retinopathy or maculopathy

Endpoints (5)

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

Other (unclassified)
3
Glycemic / diabetes
2

Glycemic / diabetes

2 endpoints
Secondary/protocol endpoint/low confidence

Beta-cell function

Time frame:Up to 92 days

descriptive

Secondary/protocol endpoint/low confidence

Overall glycemia

Time frame:Up to 95 days

descriptive, improvement

Other (unclassified)

3 endpoints
Primary/protocol endpoint/low confidence

Clock Gene expression

Time frame:Up to 95 days

descriptive

Secondary/protocol endpoint/low confidence

AMPK mRNA expression

Time frame:Up to 95 days

descriptive

Secondary/protocol endpoint/low confidence

SIRT1 mRNA expression

Time frame:Up to 95 days

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 6, 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 6, 2026 snapshot.