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magnetic stimulation of skeletal and respitatory muscle for COVID-19

Not Applicable
Conditions
COVID-19
magnetic stimulation therapy
Registration Number
JPRN-jRCTs032210201
Lead Sponsor
Sakai Tomoko
Brief Summary

The study will be terminated without being initiated due to difficulties in obtaining cases.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
0
Inclusion Criteria

Part 1:
1) Healthy persons who do not have cardiopulmonary diseases
2) Men or women more than 19years old at informed consent
3) Persons from whom informed consent were obtained with sufficient understanding and by their free will after detailed explanation on participating this study
Part 2:
1) Patients with severe COVID-19 in ICU of Tokyo Medical and Dental University
2) men or women who are more than 19 years at informed consent
3) Patients from whose proxies informed consent were obtained with sufficient understanding and by their free will after detailed explanation on participating this study ( from patients if possible)

Exclusion Criteria

1) pace-maker user
2) The patient who is judged to be inappropriate as a study subject by a study responsibility doctor and a study allotment doctor (the following study responsibility doctors)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Part I: Healthy persons<br>(Outcomes assessment)<br>The changes of the following outcomes between before with 1, 2 and 3weeks after stimulation <br>1. The muscle thickness and the muscle mass area at the center of bilateral quadriceps by ultrasonography<br>2. The thickness of diaphragm by ultrasonography<br>3. The circumference of the thighs at 5, 10, 15, 20 cm beyond the upper edge of the patella <br>Part 2: Patients with severe COVID-19 <br>(Outcomes assessment)<br>The changes of the following outcomes between before with every week to the end of sedation and the start of active movements <br>1. The muscle thickness and the muscle mass area at the center of bilateral quadriceps by ultrasonography<br>2. The thickness of diaphragm by ultrasonography<br>3. The circumference of the thighs at 5, 10, 15, 20 cm beyond the upper edge of the patella
Secondary Outcome Measures
NameTimeMethod
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