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NCT05293808: DIABE-ASACS

Platelet Aggregation in Diabetic Patients With Acute Coronary Syndrome Treated With Different Doses of Aspirin

Completed Phase 4 Last updated 23 February 2024
What this trial tests

Phase 4 trial testing aspirin 100 mg bis in die in Acute Coronary Syndrome in 60 participants. Completed in 1 January 2016.

Timeline
1 May 2014
Primary endpoint
1 October 2014
1 January 2016

Quick facts

Lead sponsorFederico II University
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date1 May 2014
Primary completion1 October 2014
Estimated completion1 January 2016
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Federico II University

Who can join

Adults 40 to 80, any sex, with Acute Coronary Syndrome or Diabetes Mellitus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Diabetes is an important risk factor of coronary atherosclerosis, and it's well known that platelets of diabetic patients are hyper reactive and so resistant to common antithrombotic therapy. Moreover, in diabetic patients platelets are characterized by high turnover that is responsible of lack of protection by cardioaspirin at common dosage. The aim of our study is to asses the efficacy of different doses of aspirin in diabetic patients with acute coronary syndrome.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Acute Coronary Syndrome

Currently open trials in the same condition.

Other Federico II University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05293808.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing