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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01459601
Other study ID # CabergolinDM
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 24, 2011
Last updated October 24, 2011
Start date January 2012
Est. completion date February 2012

Study information

Verified date October 2011
Source Mashhad University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

Diabetic patients with poorly control blood sugar are prescribed cabergoline for 1 months and their blood glucose is evaluated.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Type 2 diabetes

- HbA1C>7

Exclusion Criteria:

- HbA1C>10

- Psychiatric disorders

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Cabergoline
0,5mg per week

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mashhad University of Medical Sciences

Outcome

Type Measure Description Time frame Safety issue
Primary FBS (fasting blood sugar) 30days No
Secondary HbA1C 30days No
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