Skip to content

Telmisartan Versus Ramipril After Acute Coronary Syndrome

Telmisartan vs Ramipril for Reduction of Inflammation and Recruitment of Endothelial Progenitor Cells After Acute Coronary Syndrome

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00702936
Acronym
TERACS
Enrollment
50
Registered
2008-06-20
Start date
2007-11-30
Completion date
2008-11-30
Last updated
2008-06-20

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

Conditions

Acute Coronary Syndrome, Coronary Disease, Myocardial Infarction

Brief summary

The purpose of this study is to compare the antinflammatory and endothelial progenitor cell (EPC) mobilizing effect of Ramipril and Telmisartan in patients presenting with acute coronary syndrome

Interventions

DRUGTELMISARTAN

80 mg daily

DRUGRAMIPRIL

5 mg daily

Sponsors

Catholic University of the Sacred Heart
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Biochemical evidence of myocardial infarction as indicated by elevation of cTnT, * presence of ECG ischemic changes, * angiographic evidence of a primary coronary event, such as plaque erosion and/or rupture, fissuring, or dissection at coronary angiography, * successful coronary revascularization of at least one culprit coronary vessel.

Exclusion criteria

* Age\>80 years, current ACE inhibitor or ARB treatment, * ejection fraction \<35%, infarction secondary to ischemia due to an imbalance of O2 supply and demand, * ECG abnormalities that could affect the recognition of ST segment shift, * recent or chronic infective or inflammatory diseases, * malignancy, and myocardial infarction, * surgery or trauma in the previous month.

Design outcomes

Primary

MeasureTime frame
High sensitivity C-Reactive Protein20 days after hospital discharge

Secondary

MeasureTime frame
Endothelial Progenitor Cells20 days after hospital discharge

Countries

Italy

Contacts

Primary ContactItalo Porto, MD, PhD
i.porto@doctors.org.uk0039(0)6-30154127
Backup ContactItalo Porto, MD, PhD
italo.porto@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026