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Development of dynamic X-ray inspection technology

Not Applicable
Recruiting
Conditions
Chronic obstructive pulmonary disease
Registration Number
JPRN-jRCTs062210022
Lead Sponsor
Isobe Takeshi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
1000
Inclusion Criteria

COPD patients who are admitted or attended the Shimane University Hospital and healthy volunteers(patients without respiratory dysfunction who are admitted or attended the Shimane University Hospital, medical examination participants, Hospital staff medical examination perticipants and students)
For healthy volunteers, those who meet the following 1-3.
1.Persons aged 20 years and over at the time of consent.
2.Persons who are possible labored breathing, resting breathing and breath holding in the standing or lying position.
3.Persons who have received sufficient explanation before participating in this study, and have obtained written consent by their own free will with sufficient understanding.
For COPD patients, those who meet the following 1-4
1.Patients aged 20 years and over at the time of consent.
2.Patients who are possible labored breathing, resting breathing and breath holding in the standing or lying position.
3.Patients who have received sufficient explanation before participating in this study, and have obtained written consent by their own free will with sufficient understanding.
4. Patients who was diagnosis COPD by pulmonorogist.

Exclusion Criteria

1.Persons who do not understand the breathing instructions at the time of examination(ex;dementia)
2.Persons with a history of thoracic surgery beyond lobectomy and radiation therapy to the chest.
3.People who are currently admitting or attending the department of respiratory medicine because of respiratory dysfunction other than COPD.
4.Women who are currently pregnant, may be pregnant or breastfeeding.
5.Persons with an implantable pacemaker or implantable defibrillator.
6.Other persons who are judged to be inappropriate by the investigator and the investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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