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Jewel P-WCD Post-Approval Study (PAS)

E

Element Science

Status

Not yet enrolling

Conditions

Jewel-P WCD

Treatments

Other: This study is an observational registry study of the Jewel P-WCD in post-market use
Other: Jewel

Study type

Observational

Funder types

Industry

Identifiers

NCT07256678
PR-3162

Details and patient eligibility

About

The objective of this PAS is to demonstrate the continued safety and clinical effectiveness of the Jewel P-WCD.

Full description

This study is an observational registry study of the Jewel P-WCD in post-market use

Enrollment

6,330 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • N/A - registry will collect data already obtained commercially from patients prescribed the Jewel P-WCD.

Exclusion criteria

  • N/A - registry will collect data already obtained through commercial consent from patients prescribed the Jewel P-WCD

Trial design

6,330 participants in 1 patient group

This study is an observational registry study of the Jewel P-WCD in post-market use
Treatment:
Other: Jewel
Other: This study is an observational registry study of the Jewel P-WCD in post-market use

Trial contacts and locations

0

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Central trial contact

VP, Regulatory Affairs and Quality

Data sourced from clinicaltrials.gov

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