Last reviewed · How we verify
NCT03619395: RiskOp-ACS
Risc Optimisation- Acute cor5onary Syndrome
trial in Acute Coronary Syndrome in 150 participants. Status unknown.
1 July 2020
Quick facts
| Lead sponsor | Parc de Salut Mar |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 150 |
| Start date | 1 September 2018 |
| Primary completion | 1 July 2020 |
| Estimated completion | 1 July 2023 |
| Sites | 1 location across Spain |
Conditions studied
- Acute Coronary Syndrome — all drugs for Acute Coronary Syndrome →
- Ischemic Heart Disease — all drugs for Ischemic Heart Disease →
Sponsor
Parc de Salut Mar — full company profile →
Who can join
18 and older, any sex, with Acute Coronary Syndrome or Ischemic Heart Disease. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study evaluates the percentage of patients that reach the objective levels of LDL cholesterol, glycosylated hemoglobin and blood pressure recommended by clinical guidelines after an acute coronary syndrome, following strategies of pharmacological optimization based on algorithms. The investigators hypothesize that the use of algorithms designed and protocolized within a cardiac rehabilitation program after an ACS to optimize pharmacological treatment is effective and safe to improve the control of risk factors in patients with high cardiovascular risk.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
An intensive, structured, mobile devices-based healthcare intervention to optimize the lipid-lowering therapy improves lipid control after an acute coronary syndrome.
Ruiz-Bustillo S, Badosa N, Cabrera-Aguilera I, Ivern C, et al · · 2022 · cited 3× · PMID 35958430 · DOI 10.3389/fcvm.2022.916031 -
Prognostic Utility of a New Risk Stratification Protocol for Secondary Prevention in Patients Attending Cardiac Rehabilitation.
Cabrera-Aguilera I, Ivern C, Badosa N, Marco E, et al · · 2022 · cited 3× · PMID 35407518 · DOI 10.3390/jcm11071910
Verify or expand the search:
- PubMed search for NCT03619395
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other Parc de Salut Mar trials
Trials by the same sponsor.
- NCT06163235 — Efficacy of a Mobile Application and Semi-attendance Program in Bariatric Surgery · NA · not yet recruiting
- NCT07223450 — A Study on Oral and Intranasal Forms of Oxycodone in Healthy Volunteers Using Pharmacokinetic Modeling · Phase 1 · completed
- NCT07504913 — Spanish Validation of KOQUSS-40 Questionnaire: Assessing QoL of Gastric Cancer Patients After Gastrectomy: SPQUSS-41 · recruiting
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- NCT04084795 — Augmentation of EMDR With tDCS in the Treatment of Fibromyalgia · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03619395 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Parc de Salut Mar
- Last refreshed: 6 September 2019
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/NCT03619395.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing