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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01007474
Other study ID # MDT-OHCS
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 2004
Est. completion date January 2030

Study information

Verified date February 2021
Source Medtronic Italia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The One Hospital ClinicalService Project is an integrated system composed by a network of International Hospital Departments, a clinical data repository and a shared environment for the collection, management, analysis and reporting of clinical and diagnostics data from patients treated by Medtronic therapies or patients wearing Medtronic implantable devices used within their intended use. The One Hospital ClinicalService is composed by a suite of systematic, data-guided activities designed to bring about immediate improvements in health delivery in particular settings. Data are prospectively collected. An independent committee of physicians prospectively identifies key clinical questions on a yearly basis for development of quality improvement activities, analyses and publications. A charter, approved by Hospital Istitutional Review Boards or other Hospital entities, assigns the ownership of data to the centers and governs the conduct of the project and the relationship of the scientific committee and Medtronic. Hospital is the data controller, while Medtronic is the data processor on behalf of the Hospital. Data collected for quality improvement purposes may be mined to perform clinical research.


Description:

One Hospital ClinicalService is a project aiming to provide information and analysis of clinical and device data, back to the treating healthcare providers regarding their own patients, in order to help those healthcare providers improve outcomes and understanding of their patients' care or patients' management. The mission of the One Hospital ClinicalService Project is to improve outcomes and comprehension of diagnostic and therapeutic strategies applied to patients wearing Medtronic implantable devices or treated by Medtronic therapies. One Hospital ClinicalService provides services to evaluate and improve the quality of clinical care in the International clinical practice. One Hospital ClinicalService collects acute and chronic patient and device data in a large population during routine usage of the device, without specific study interventions, and always within the approved intended use of the device. One Hospital ClinicalService uses a core database which can be expanded with specific data sets for particular patient populations, diseases, therapies, devices or features. One Hospital ClinicalService, with its prospective data collection and its data management infrastructure, forms a data-bank where physicians collect patient data and from which they receive reports about clinical and device diagnostics data. Usage and understanding of diagnostics data may help physicians to optimize tailor device programming and patient therapies. This data-bank, queried by retrospective statistical analyses, may help physicians in quality improvement activities, education, research and scientific activities. Some examples of scientific focus available through the One Hospital ClinicalService Project include: - Describing the use of implantable devices, such as cardioverter defibrillator (ICD), pacemakers, implantable loop recorders or others in the Italian clinical practice - Identifying predictors or clinical variables correlated with clinical outcomes or therapy response - Evaluating and testing methods to optimize device programming and patient therapy via device diagnostics or patient reports


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 2030
Est. primary completion date January 2028
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients wearing a Medtronic market-released device or treated by a Medtronic therapy who have signed a patient data release and informed consent form Exclusion Criteria: - Patients unwilling or unable to cooperate or give voluntary consent

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Implantable Cardioverter-Defibrillator (ICD)
Medtronic market-released implantable cardioverter-defibrillator
Implantable Pacemaker Generator (IPG)
Medtronic market-released implantable pacemaker generator
Implantable Loop Recorder (ILR)
Medtronic market-released implantable loop recorder
Cardiac Resynchronization Therapy-Defibrillator (CRT-D)
Medtronic market-released cardiac resynchronization therapy defibrillator
Implantable devices working as neurostimulators, stents, spinal/bone devices or other applications
Medtronic market-released implantable devices used as neurostimulators, stents, spinal/bone devices or for other applications

Locations

Country Name City State
Germany Stauferklinikum Mutlangen Mutlangen
Iceland Landspitali University Hospital Reykjavík
India Eternal Hospital Jaipur
India Fortis Escort Heart Institute New Delhi
Italy S.Orsola Malpigli Bologna
Italy Ospedale Civile di Bolzano Bolzano
Italy A.O. S.Sebastiano di Caserta Caserta
Italy S. Anna Hospital Como
Italy A.O. Santa Croce e Carle Cuneo
Italy Ospedale Santa Croce Fano
Italy A.Ospedaliero Universitaria Careggi Firenze
Italy Ospedali Riuniti Leonardi-Riboli Lavagna
Italy ASL 2 Avellino Mercogliano
Italy Istituto Auxologico Italiano Milano
Italy Istituto Ca' Granda-Niguarda Milano
Italy Ospedale Luigi Sacco Milano
Italy San Carlo Borromeo Milano
Italy Ospedale Sacro Cuore Don Calabria Negrar
Italy A.O. di Parma Parma
Italy Policlinico S. Matteo Pavia
Italy A.O. San Salvatore di Pesaro Pesaro
Italy Arcispedale Santa Maria Nuova Reggio Emilia
Italy Fatebenefratelli S:Giovalli Calibita Roma
Italy Policlinico A. Gemelli Roma
Italy San Filippo Neri Hospital Roma
Italy Istituto Clinico Humanitas Rozzano
Italy ASL Teramo Teramo
Italy A.O. S.Maria della Misericordia Udine
Italy Ospedale S. Maria della Misericordia Urbino
Japan Tokyo Medical and Dental University Hospital Bunkyo-Ku Tokyo
Japan Kagawa University Hospital Kagawa
Japan Saiseikai Kawaguchi General Hospital Kawaguchi
Japan Osaka University Hospital Suita Osaka
Japan Toyohashi Heart Center Toyohashi
Saudi Arabia King Fadh Atmnd Forces Hospital Jeddah
Saudi Arabia Prince Sultan Cardiac Center Riyadh
South Africa Mediclinic Panorama Hospital Cape Town
Sweden Hallandssjukhus Varberg Varberg
United Kingdom Blackpool Victoria Hospital Blackpool
United Kingdom Greater Glasgow Health Board Glasgow
United Kingdom Central Manchester University Hospital NHS Foundation Trust Manchester

Sponsors (2)

Lead Sponsor Collaborator
Medtronic Italia Medtronic

Countries where clinical trial is conducted

Germany,  Iceland,  India,  Italy,  Japan,  Saudi Arabia,  South Africa,  Sweden,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Other Device interventions 10 years
Primary Mortality 10 years
Secondary Hospitalizations 10 years
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