Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03115723
Other study ID # CHUBX 2014/29
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 15, 2016
Est. completion date January 15, 2017

Study information

Verified date February 2022
Source University Hospital, Bordeaux
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Hospital readmission rate following percutaneous coronary interventions (PCI) or coronary angiographies (CAG) is a main indicator of quality of care and addresses economic issues. The aim of this study is to quantify the frequency and analyse the types of rehospitalizations and repeat revascularizations during one year after a PCI or a CAG. This information is needed to organize the health care pathway and to identify preventable rehospitalizations.


Recruitment information / eligibility

Status Completed
Enrollment 11487
Est. completion date January 15, 2017
Est. primary completion date January 15, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients included in ACIRA Registry : All volunteer adults (= 18 years) and French resident patients who underwent PCI and CAG in the interventional cardiology hospitals in the Aquitaine region (France), - Initial PCI or CAG performed from January 1, 2012 to December 31, 2013, - Initial PCI or CAG performed in nine interventional cardiology hospitals in the Aquitaine region (France). Exclusion Criteria: - Patients who declined to take part of ACIRA Registry, - Patients resident outside the Aquitaine region (France), - Patients who died during the initial hospital stay, - Patients hospitalized for a PCI or a CAG the month preceding the initial procedure including in the ACIRA-Rehosp study.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Percutaneous coronary intervention

Coronary angiography


Locations

Country Name City State
France Clinique Esquirol St Hilaire Agen
France Clinique cardiologique d'Aressy Aressy
France GCS Bayonne Bayonne
France Clinique de Caudéran les pins-francs Bordeaux
France Clinique de St Augustin Bordeaux
France CH de Libourne Libourne
France CH de Mont de Marsan Mont de Marsan
France CH de Pau Pau
France CH de Perigueux Perigueux
France CHU de Bordeaux Pessac
France Hôpital privé St Martin Pessac

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Type of rehospitalization Baseline to 1 year
Primary Number of rehospitalization Baseline to 1 year
Secondary Identification of hospitals All hospitals concerned by initial coverage and rehospitalization Baseline to 1 year
Secondary Type of diagnoses and procedures associated with each type of rehospitalization Baseline to 1 year
Secondary Type of cardiac rehabilitation procedures in hospitalizations for post-operative and rehabilitation wards Baseline to 1 year
See also
  Status Clinical Trial Phase
Completed NCT01239225 - Prevalence of Abdominal Aortic Aneurysm in Patients Undergoing Coronary Angiography Phase 4
Recruiting NCT05075590 - Coronary Access After Supra-Annular THV Implantation N/A
Completed NCT02606734 - DyeVert Pilot Trial N/A
Completed NCT00632918 - Effects of Heart Rates and Variability of Heart Rates on Image Quality of Dual-Source CT Coronary Angiography N/A
Completed NCT04801901 - Distal Transradial Access for Percutaneous Coronary Intervention N/A
Completed NCT00345501 - Iloprost for Prevention of Contrast-Mediated Nephropathy in High-Risk Patients Undergoing Coronary Angiography and/or Intervention Phase 2/Phase 3
Recruiting NCT04521660 - The Effect of Using Virtual Reality Glasses During Coronary Angiography N/A
Completed NCT05982366 - Feasibility and Safety of the Routine Distal Transradial Approach N/A
Recruiting NCT04982419 - Remote Ischemic Preconditioning for Renal and Cardiac Protection in Congestive Heart Failure (RICH) Trial Phase 2/Phase 3
Completed NCT00468325 - Coronary Computed Tomography for Systematic Triage of Acute Chest Pain Patients to Treatment (CT-STAT) N/A
Completed NCT00468195 - Optimizing Image Quality in Obese Patients Undergoing Coronary Computed Tomography (CT) Angiography N/A
Completed NCT04911218 - GlideSheath Slender® Versus Conventional 5Fr Arterial Sheath in Coronary Angiography Through the Distal Radial Artery N/A
Completed NCT04318990 - DIstal vs Proximal Radial Artery Access for Cath N/A
Recruiting NCT06312397 - The Effect on Back Pain and Fatigue Level of Acupressure N/A
Recruiting NCT05319119 - Fractional Flow Reserve Derived From CT Related Treatment
Not yet recruiting NCT05133206 - Fasting or Non-fasting Before Cardiac Catheterization N/A
Completed NCT02818101 - Hypnosis Efficacy for the Prevention of Anxiety During a Coronary Angiography N/A
Completed NCT00465335 - Usefulness of Coronary CT Angiography in Patients With Inconclusive Stress Test Results N/A
Recruiting NCT06035783 - Calcium Reduction by Orbital Atherectomy in Western Europe
Completed NCT04407936 - Risk Factors and Prognosis of Adverse Cardiovascular and Kidney Events After Coronary Intervention