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Study to Determine Presence of Prediabetes in Subjects with Cardiovascular Disease

Study to Determine Presence of Prediabetes in Subjects with Cardiovascular Disease - Prescreening Pilot

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON42994
Enrollment
70
Registered
2016-10-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

diabetes increased blood sugar

Interventions

All subjects meeting the inclusion and exclusion criteria in Group A will be contacted and asked if they are interested in participating in a future potential clinical study. If they have interest o

Sponsors

Janssen-Cilag
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Man or woman of *18 years of age * Documented symptomatic atherosclerotic CV disease including a history of one of the following: * Stroke * Myocardial infarction * Hospitalized admission for unstable angina * Percutaneous coronary intervention (with or without stenting) * Peripheral revascularization (angioplasty or surgery) JNJ-28431754 Clinical Protocol 28431754PRD0001 5 Approved, Date: 29 March 2016 * Symptomatic with documented hemodynamically significant carotid or peripheral vascular disease

Exclusion criteria

Exclusion criteria: * History of T2DM, type 1 diabetes mellitus, latent autoimmune diabetes in adults (LADA), diabetic ketoacidosis * History of hereditary glucose-galactose malabsorption or primary renal glycosuria * History of use of a glucose lowering drug (other than short-term use during a hospitalization or for gestational diabetes; or subjects with a history of gestational diabetes may be included if at least 3 months has passed since the discontinuation of a glucose lowering drug)

Design outcomes

Primary

MeasureTime frame
* support the assessment of the feasibility of conducting a clinical study in this population, and * identify subjects with CV disease and prediabetes who might have interest in participating in a future clinical study.

Secondary

MeasureTime frame
/

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)