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Clinical Trials/NCT03875222
NCT03875222UnknownNot Applicable

Studying New Criteria for Prediction of Site of Accessory Pathway From Surface ECG

Assiut University0 sites50 target enrollmentStarted: April 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
50
Primary Endpoint
percise localization of accessory pathway from surface ECG in referance to successful ablation site

Study Overview

Brief Summary

study for discovering new criteria for localization of site of accessory pathway from surface ECG

Detailed Description

the study aims for discovering new criteria for percise localization of accessory pathway from surface ECG in referance to final flouroscopic ablation site

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
10 Years to 90 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • any patient with manifest accessory pathway .

Exclusion Criteria

  • multiple accessory pathways .previous ablation.

Outcomes

Primary Outcomes

percise localization of accessory pathway from surface ECG in referance to successful ablation site

Time Frame: 2 years

successful localization of accessory pathway from surface ECG in referance to successful ablation site during EP maping

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Haidy Yacoup Daoud Danial

principle investigator

Assiut University

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