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Pedicor Trial s.r.o.

Verified siteinfo

Czechia Horni 266/73, Dubina, 700 30 Ostrava, Czechia

  • 1 trial recruiting
  • Arteriosclerosis · Atrial fibrillation · Cardiovascular disorder
  • Adult patients

About Specializations

Pedicor Trial s.r.o. in Ostrava, Czechia specialises in clinical trials of conditions such as Arteriosclerosis, Atrial fibrillation, Cardiovascular disorder, Dyslipidaemia, and other specialisations. This site conducts important research.

Main research areas of the site

Cardiovascular Disease Research

The site focuses on cardiovascular diseases, investigating treatments aimed at reducing major adverse cardiac events in patients with established disease or high risk.

  • Evaluation of novel oral agents for MACE reduction
  • Assessment of cardiovascular outcomes in high‑risk populations
  • Study of atherosclerotic disease progression

Pedicor Trial s.r.o. conducts these studies within its cardiology and angiology department, seeking safer and more effective therapies for heart and vascular health.

Hypertension and Heart Failure Prevention

Research also targets hypertension and its impact on heart failure, testing innovative therapies that may lower blood pressure and prevent cardiovascular death.

  • Investigation of RNA‑based treatments for resistant hypertension
  • Analysis of hospitalization rates for heart failure
  • Comparison of new agents versus placebo in stroke risk reduction

The studies aim to improve management of patients with uncontrolled blood pressure and reduce the burden of cardiovascular complications across Ostrava and beyond.

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Site location
Horni 266/73, Dubina700 30 OstravaCzechia
Recruiting now
1 trial
Conditions studied
7
Partner status
Verified site

More sites in OstravaCzechia

Recruiting now

Ongoing trials

Clinical trials currently enrolling participants at this site.

Condition
Type of trial
Recruitment status
Quick filters

6 clinical trials

Study of Zilebesiran Added to Standard Treatment to Reduce Heart Problems in Adults with High Blood Pressure and Heart Disease Risk

Investigational
Countries:CzechiaCzechia
  • Participants:18–64 years · 65+ years
  • Substances:Zilebesiran
  • Sponsor:Alnylam Pharmaceuticals Inc.

Efficacy and Safety of REGN7508, REGN9933, and Rivaroxaban in Adults with Peripheral Artery Disease after Recent Lower‑Extremity Revascularization

Registered drug
Countries:CzechiaCzechia
  • Participants:18–64 years · 65+ years
  • Substances:REGN7508
  • Sponsor:Regeneron Pharmaceuticals Inc.

Atrial fibrillation

Not yet recruiting

Prevention of Stroke and Systemic Embolism in Atrial Fibrillation Patients Treated with REGN7508 (cenvacibart) versus Apixaban

Registered drug
Countries:CzechiaCzechia
  • Participants:18–64 years · 65+ years
  • Substances:Apixaban
  • Sponsor:Regeneron Pharmaceuticals Inc.

Arteriosclerosis

Not recruiting

A study to evaluate the effect of olpasiran on major cardiovascular events in patients with atherosclerotic cardiovascular disease and high levels of lipoprotein(a)

Investigational
Countries:CzechiaCzechia
  • Participants:18–64 years · 65+ years
  • Sponsor:Amgen Inc.

Myocardial infarction

Not recruiting

Study of Orticumab in Adults with Previous Heart Attack and High Coronary Inflammation Measured by CT Scan

Investigational
Countries:CzechiaCzechia
  • Participants:18–64 years · 65+ years
  • Substances:Orticumab
  • Sponsor:Abcentra LLC

Dyslipidaemia

Not recruiting

Study of Evolocumab to Prevent Heart Disease Events in High-Risk Patients Without Previous Heart Attack or Stroke

Registered drug
Countries:CzechiaCzechia
  • Participants:18–64 years · 65+ years
  • Substances:Evolocumab
  • Sponsor:Amgen Inc.
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