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NCT04930302: PHAROS
Optimizing the Pharmacotherapy of Vascular Surgery Patients at Hospital Admission, at Discharge and at Post-discharge Check-up: Quasi-experimental Clinical Uncontrolled Trial (PHAROS)
trial in Medication Errors and Other Product Use Errors and Issues in 105 participants. Completed in 1 October 2023.
30 September 2022
Quick facts
| Lead sponsor | National Institute of Cardiovascular Diseases, Slovakia |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 105 |
| Start date | 1 September 2021 |
| Primary completion | 30 September 2022 |
| Estimated completion | 1 October 2023 |
| Sites | 1 location across Slovakia |
Conditions studied
- Medication Errors and Other Product Use Errors and Issues — all drugs for Medication Errors and Other Product Use Errors and Issues →
Sponsor
National Institute of Cardiovascular Diseases, Slovakia
Who can join
18 and older, any sex, with Medication Errors and Other Product Use Errors and Issues. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This project aims to assess the impact of pharmaceutical care in collaboration with physicians on prevalence of DRPs at hospital admission and discharge in patients with carotid artery disease or lower extermity artery disease hospitalized at the Department of Vascular Surgery. The key focus area of this project will be the identification of DRPs, their occurrence and type. As a part of further research, the investigators want to analyze the a) acceptance rate of pharmaceutical intervention by physicians. Proportion of accepted interventions by physicians was calculated and b) patients' understanding of his/her pharmacotherapy assessed on a three-point scale at hospital admission. Hypothesis: Null hypothesis: Pharmaceutical care provided at hospital admission and at hospital discharge does not reduce prevalence rates of DRPs in patients with carotid artery disease or lower extermity artery disease hospitalized at the Department of Vascular Surgery. Alternative hypothesis: Pharmaceutical care provided at hospital admission and at hospital discharge reduces prevalence rates of DRPs in patients with carotid artery disease or lower extermity artery disease hospitalized at the Department of Vascular Surgery. Primary outcomes: Change in the prevalence rate of DRPs at hospital admission vs. hospital discharge. Secondary outcomes: 1. acceptance rate of pharmaceutical intervention by physician 2. patients' understanding of his/her pharmacotherapy
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Pharmacist-led interventions for vascular surgery patients: a prospective study on reducing drug-related problems.
Porubcova S, Szmicsekova K, Lajtmanova K, Slezakova V, et al · · 2024 · cited 4× · PMID 39695586 · DOI 10.1186/s12913-024-12015-7 -
Optimizing the Pharmacotherapy of Vascular Surgery Patients at Hospital Admission and Discharge (PHAROS): Protocol for a Quasi-Experimental Clinical Uncontrolled Trial.
Porubcova S, Lajtmanova K, Szmicsekova K, Slezakova V, et al · · 2025 · PMID 40106812 · DOI 10.2196/60728
Verify or expand the search:
- PubMed search for NCT04930302
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Related trials
Other National Institute of Cardiovascular Diseases, Slovakia trials
Trials by the same sponsor.
- NCT05827120 — Endovascular Therapy in Patients With Acute Deep Vein Thrombosis · completed
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 NCT04930302 (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 National Institute of Cardiovascular Diseases, Slovakia
- Last refreshed: 11 October 2023
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/NCT04930302.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing