Optimal EGM Configuration for Morphology Discrimination

Clinical Trial Summary

The study will be a prospective cohort study of 20 patients recruited from site's Defibrillator Clinic patient population who are followed at the site.

Hypothesis: Among the available EGM configuration options, one is better than the others for detection enhancements purposes.

See also
	Status	Clinical Trial	Phase
	Enrolling by invitation	`NCT05903313` - A Study to Evaluate Accuracy and Validity of the Chang Gung ECG Abnormality Detection Software
	Recruiting	`NCT04415203` - TAES for FPVCs: a Pragmatic, Randomized Controlled Trial	N/A

See also

Status

Clinical Trial

Phase

Enrolling by invitation

NCT05903313 - A Study to Evaluate Accuracy and Validity of the Chang Gung ECG Abnormality Detection Software

Recruiting

NCT04415203 - TAES for FPVCs: a Pragmatic, Randomized Controlled Trial

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00888667
Study type	Observational
Source	Abbott Medical Devices
Contact
Status	Terminated
Phase
Start date	April 2009
Completion date	May 2010

Optimal EGM Configuration for Morphology Discrimination — SVT Morphology

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms