MedTrace Logo

CT Guided WiSE-CRT

NCT03495505 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2022-03-29

No results posted yet for this study

Summary

This feasibility study will use CT scanning to identify the optimal location for placement of the WiSE-CRT system.

Conditions

Interventions

DEVICE

WiSE-CRT

Intervention will involve placement of the WISE-CRT system which consists of a transmitter, battery and electrode.

Sponsors & Collaborators

  • National Institute for Health Research, United Kingdom

    collaborator OTHER_GOV

  • Guy's and St Thomas' NHS Foundation Trust

    lead OTHER

Principal Investigators

  • Steven Niederer, DPhil · King's College London

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-08-31
Primary Completion
2021-05-05
Completion
2021-05-05

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03495505 on ClinicalTrials.gov