Safety and feasibility of hospital discharge 2 days following primary percutaneous intervention for ST-segment elevation myocardial infarction.
Daniel A Jones, Krishnaraj S Rathod, James Philip Howard...
https://pubmed.ncbi.nlm.nih.gov/23053711Actively Recruiting
Led by Queen Mary University of London · Updated on 2026-02-27
20000
Participants Needed
2
Research Sites
8 weeks
Total Duration
Coronary artery disease (CAD) remains a leading cause of death worldwide despite improvements over time. Advances in minimally invasive treatments have improved patient outcomes, but real-world data on intervention and treatment safety and effectiveness are needed. This research focuses on patients with acute coronary syndrome discharged early after primary percutaneous coronary intervention (PCI) to better understand their characteristics and outcomes, helping improve risk assessment and care strategies. The study uses a large clinical database from a major cardiac center in Europe, including patients admitted with acute coronary syndrome and discharged early after PCI. This observational registry collects demographic, clinical, and outcome data on patients with a range of CAD complexities. The research aims to assess the safety and feasibility of the early discharge pathway and explore predictors of outcomes and complications following interventional treatment. Participants' data are collected and analyzed over one year, including medication adjustments, major adverse cardiac events, and quality of life assessments. The study uses secure databases and monitors patient outcomes to provide real-world evidence on early discharge after heart attack treatment. The findings intend to inform local and global care practices and stimulate further research in underexplored areas of cardiac care.
CONDITIONS
Early Discharge Pathway Registry
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 year
Participants who undergo routine care are observed after discharge via the early discharge pathway at Barts Heart Centre. Data on their health status, medication titration, and quality of life are collected.
Regular follow-up visits as per routine care
Total: 2 locations
1
Barts Health NHS Trust
London, United Kingdom
Actively Recruiting
2
Dr. Daniel Jones
London, United Kingdom
Actively Recruiting
D
Dr. Daniel A Jones
D
Dr. Krishnaraj S Rathod
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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