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Co-administration of Cabergoline and Gliclazide Improve Glycemic Parameters and Lipid Profile in T2DM Patients

S

Sherief Abd-Elsalam

Status and phase

Unknown
Phase 3

Conditions

Diabetes

Treatments

Drug: Cabergoline
Drug: Gliclazide

Study type

Interventional

Funder types

Other

Identifiers

NCT03313661
Diabetes Mellitus

Details and patient eligibility

About

Evaluation of the glycemic efficacy of cabergoline on diabetic patients

Full description

Type 2 diabetes mellitus (DM) is a progressive metabolic disorder that is associated with basal hyperinsulinemia, insulin resistance and impaired insulin release. Glycemic control is a fundamental part of the management of type 2 DM and difficult to achieve. Different antidiabetic agents can handle diabetic metabolic abnormalities. The development of antidiabetic agentswith novel mechanisms of action is highly desirable. Cabergoline, a long acting D2 agonist, is expected to play a role in the glycemic control.

Enrollment

60 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Diabetic patients.

Exclusion criteria

  • Other drugs administration

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 3 patient groups

Cabergoline
Experimental group
Description:
cabergoline 0.5 mg twice weekly within 2 hrs of awakening plus gliclazide
Treatment:
Drug: Cabergoline
Gliclazide
Active Comparator group
Description:
gliclazide (60-120 mg) once daily
Treatment:
Drug: Gliclazide
Placebo
No Intervention group
Description:
Placebo

Trial contacts and locations

1

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Central trial contact

Sherief Abd-Elsalam, consultant

Data sourced from clinicaltrials.gov

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