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Terminated Not applicable Interventional Results available

Wearable Cardioverter Defibrillator in Hemodialysis Patients (WED-HED) Study

ClinicalTrials.gov ID: NCT02481206

Public ClinicalTrials.gov record NCT02481206. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 2:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A multi-center, prospective, randomized controlled clinical trial with 1:1 assignment of treatment and control. This study will evaluate the impact of wearable cardioverter defibrillator use on sudden cardiac death in incident hemodialysis patients. The study will enroll up to 2,600 subjects. A maximum of 200 sites in the USA will be used for enrollment.

Study identification

NCT ID
NCT02481206
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Zoll Medical Corporation
Industry
Enrollment
66 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2015 (Type not available)
Primary completion
Dec 2017 (Actual)
Completion
Dec 2017 (Actual)
Last update posted
Jan 19, 2021

2015 – 2017

United States locations

U.S. sites
31
U.S. states
17
U.S. cities
31
Facility City State ZIP Site status
Not listed Corona California — —
Not listed Downey California — —
Not listed Escondido California — —
Not listed Los Angeles California — —
Not listed Sacramento California — —
Not listed San Dimas California — —
Not listed San Luis Obispo California — —
Not listed Whittier California — —
Not listed Stamford Connecticut — —
Not listed Hialeah Florida — —
Not listed Miami Florida — —
Not listed Pembroke Pines Florida — —
Not listed Winter Garden Florida — —
Not listed Albany Georgia — —
Not listed Columbus Georgia — —
Not listed Fort Wayne Indiana — —
Not listed Greenbelt Maryland — —
Not listed Detroit Michigan — —
Not listed Rochester Hills Michigan — —
Not listed Minneapolis Minnesota — —
Not listed Kansas City Missouri — —
Not listed Las Vegas Nevada — —
Not listed New Brunswick New Jersey — —
Not listed The Bronx New York — —
Not listed Durham North Carolina — —
Not listed Canton Ohio — —
Not listed Greenville South Carolina — —
Not listed Chattanooga Tennessee — —
Not listed Knoxville Tennessee — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02481206, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 19, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02481206 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →