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Treating Aspirin Resistance with GuidEd Therapy in Diabetes (TARGET-Diabetes) Study

Phase 4
Recruiting
Conditions
aspirin resistance
type 2 diabetes
Cardiovascular - Coronary heart disease
Metabolic and Endocrine - Diabetes
Registration Number
ACTRN12611001132932
Lead Sponsor
RMIT University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
400
Inclusion Criteria

Impaired fasting glucose IFG (110 – 125 mg / dL) or;
Impaired glucose tolerance IGT (140 – 199 mg / dL) or;
Type-2 diabetes (IFG > 135 mg / dL or IGT > 200 mg / dL)

Exclusion Criteria

salicylate or thienopyridine allergy or intolerance, history of haemorrhagic stroke, aneurysm or any stroke < 3 months, any thienopyridine < 3 days, history of low platelet count, history of bleeding diathesis, clinical findings in the judgement of the investigator associated with increased risk of bleeding, oral anticoagulation or other antiplatelet therapy, history of withdrawal from study due to non-compliance with medication, any condition associated with poor treatment compliance, including alcoholism, mental illness, or drug dependence, investigative site personnel directly affiliated with the study or immediate family, presently enrolled in another drug study, women who are known to be pregnant, have given birth within the past 90 days, or are breast feeding, concomitant medical illness that in the opinion of the investigator is associated with reduced survival over the expected treatment period, known severe hepatic dysfunction, planned travel or other reason why participant might be unable to cooperate with protocol requirements during the study medication period.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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