NCT03823547Recruiting
Future Optimal Research and Care Evaluation
Future Optimal Research and Care Evaluation: On the Way to "Personalized Medicine" With an Ongoing Registry of Patients in Daily Clinical Practice (Hart Beter/ FORCE-ACS)
Source: ClinicalTrials.gov · Last updated 30 Jan 2019 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Rationale: Acute coronary syndrome (ACS) is the leading cause of death worldwide. To improve cardiovascular care, research is needed. Current guidelines are mainly based on well controlled RCT's, though evaluation of the impact of such RCT's in the real world is missing. In order to evaluate the impact and to overcome certain limitations of RCT's, a more practical approach is required. In this sense the use of nonrandomized observational studies is an important tool for determining the effectiveness of a therapy in routine clinical practice. One way to gain insight in characteristics of patients presenting in daily clinical practice, is to simply register these characteristics in a prospective manner with adequate follow up. Objective: To create an ongoing registry for evaluation of clinical long-term impact of diagnostics, various treatments and devices used for ACS, for research and evaluation of quality of care and to evaluate and improve regional quality of care and cooperation between PCI and non-PCI centers.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 99999 (estimated)
- First submitted
- 25 Jan 2019
- Start date
- 1 Jan 2015
- Primary completion date
- 30 Jun 2050
- Lead sponsor
- J.M. ten Berg
- Diseases
- Coronary artery disease
- NCT number
- NCT03823547
What you commit to
- Study type: Observational
- Planned participants: 99999
- From 1 Jan 2015 to the primary completion date, 30 Jun 2050
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- No oral or signed informed consent available.
Who the study is looking for
- All patients presenting with ACS
- Age ≥ 18 years
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Gelre Ziekenhuizem Coordinator of this site? Confirm its status | Apeldoorn | Netherlands | Recruiting |
| Rijnstate Arnhem Coordinator of this site? Confirm its status | Arnhem | Netherlands | Recruiting |
| Gelderse Vallei Coordinator of this site? Confirm its status | Ede | Netherlands | Recruiting |
| Ziekenhuis Rivierenland Coordinator of this site? Confirm its status | Tiel | Netherlands | Recruiting |
Related publications
- Genotype-Guided P2Y12-Inhibitor De-Escalation Strategy in Acute Coronary Syndrome: Observational Evidence From the POPular-GUIDE PCI.Circ Cardiovasc Interv · 2026 · PMID 41744086
This page is information, not medical advice. Discuss any trial with your doctor.