Skip to content

Double blind, placebo-controlled trial to asses Cabergoline effects in type 2 diabetes

Double blind, placebo-controlled trial to asses Cabergoline effects in type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205053176N2
Enrollment
40
Registered
2012-05-21
Start date
2012-09-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes mellitus. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention:Patients randomized to double-blind treatment will be with cabergoline 5 / 0 mg once a week for three months. Intervention 2: Contro:Patients randomized to double-blind tr
Treatment - Drugs
Intervention:Patients randomized to double-blind treatment will be with cabergoline 5 / 0 mg once a week for three months
Contro:Patients randomized to double-blind treatment will be with Placebo 5 / 0 mg once a week for three months

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria :Type 2 diabetes diagnosed at least three months prior to study entry? greater than or equal treatment 2 Oral medication to control blood sugar With at least 50% of recommended dose? Age between 20 to 80 years; A1C hemoglobin more than %7.5 at the time of study entry? Reliable method of contraception in women of reproductive age entered the study. Exclusion criteria: Unwillingness of the patient? known immunodeficiency? pregnancy and lactation, cardiovascular disease? taking drugs that have effects on blood sugar levels include: corticosteroids and thiazide?Uncontrolled thyroid disease?History of diabetic ketoacidosis-Creatinine above 2-Liver and kidney disease? known allergy to cabergoline?proliferative retinopathy; HA1C >10% and severe weight loss

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cabergoline effects on glycemic control. Timepoint: After the first and second trimester of intervention. Method of measurement: Blood tests.

Secondary

MeasureTime frame
Serum Insulin. Timepoint: Before Intervention and the end of each three Months afterIntervention. Method of measurement: Blood test.;Prolactin. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Blood test.;Hypertension. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Barometer.;Weight. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Balance.;Waist size. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Meter.;Blood Urea Nitrogen. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Blood test.;Creatinine. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Blood test.;Aspartate Aminotransferase. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Blood test.;Alanine Aminotransferase. Timepoint: Before Intervention and the end of each three Months after Intervention. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Adeleh Bahar

Mazandaran University of Medical Sciences

abahar@mazums.ac.ir; Doctor_bahar2000@yahoo.com+98 15 1325 7230

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026