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Japanese

Jan. 11, 2022

April. 02, 2024

jRCTs032210543

Examination of the usefulness of a dynamic flat-panel detector system for patients with chronic pulmonary obstructive disease under the treatment with Tiotropium/Olodaterol

Evaluation of the efficacy of Tiotropium/Olodaterol by a dynamic flat-panel detector system

Ikari Jun

Chiba university hospital

1-8-1 Inohana Chuo-ku Chiba, Chiba, Japan

+81-43-222-7171

junikari@chiba-u.jp

Ikari Jun

Chiba university hospital

1-8-1 Inohana Chuo-ku Chiba, Chiba, Japan

+81-43-222-7171

junikari@chiba-u.jp

Recruiting

Jan. 11, 2022

Aug. 26, 2022
35

Interventional

single arm study

open(masking not used)

uncontrolled control

single assignment

diagnostic purpose

1) Patients diagnosed with chronic pulmonary disease (COPD) who have been or are going to be treated with medical therapy
2) Patients aged 40 to 85 at the time of obtaining consent
3) Both male and female are eligible.
4) Patients who have smoked more than 10 pack-years
5) Patients with airway obstruction with a post-bronchodilator FEV1 <80% of predicted normal , FEV1 >30%of predicted normal and FEV1/FVC <70%
6) Patients who can perform forced breathing, rest breathing and breath holding in standing position
7) Written informed consent

1) Patients with a history of asthma or currently diagnosed with asthma
2) Patients who cannot perform pulmonary function testing properly (including the history of pulmonary resection)
3) Patients with impaired mobility, including walking ability, by limb dysfunction or with bone fracture
4) Patients who have experienced exacerbation of COPD within 1 month
5) Patients with tachycardia more than 100 beats per min or life-threatening arrhythmia
6) Patients who have experienced acute myocardial infarction or have history of hospital admission for heart failure, within 1 year
7) Patients who have history of cancer (excluding basal cell carcinoma, squamous epithelial skin cancer, Endoscopic mucosal resection for gastrointestinal tumors). (However, this excludes cases where it is expected that there will be no recurrence of cancer requiring treatment during the period of participation in this study, with PS 0 at the time of registration of this study at the discretion of a specialist, and there is no problem with walking.)
8) Patients who do not understand the purpose and method of research
9) Patients with obvious dementia
10) Patients who are being treated for depression or neurosis (scores are not used, at the discretion of the doctor)
11) Patients with angle-closure glaucoma, dysuria due to benign prostatic hyperplasia, patients with a history of hypersensitivity to atropine and its related substances or components of this drug
12) Pregnant or lactating women, women who can become pregnant but cannot use contraception
13) Patients who are judged to have difficulty with temporary suspension of medication when taking LAMA or LABA
14) Patients who are judged by the principal investigator or subinvestigator to be inappropriate as the target person

40age old over
85age old under

Both

Chronic Obstructive Pulmonary Disease

Conducting X-ray dynamic image inspection by a dynamic flat-panel detector system, chest CT, administration of tiotropium/olodaterol

Dynamic-Ventilatory Digital Radiography,COPD,tiotropium/olodaterol

X-ray dynamic image inspection by a dynamic flat-panel detector system, chest CT, tiotropium/olodaterol

D029424

D013902, D061330, C000611386

Rate of change in surface area

Excursion of diaphragm
Motion speed of diaphragm
Tracheal diameter change
Tracheal narrowing rate
Maximum Pixel Change Rate
Pulmonary function testing
BDI/TDI score
CAT score
Frequency of adverse events
Equipment malfunction
ventilation, perfusion, ventilation-perfusion ratio
Chest CT parameters

Nippon Boehringer lngelheim Co. Ltd.
Not applicable
Chiba University Certified Clinical Research Review Board
1-8-1 Inohana Chuo-ku Chiba, Chiba, Japan, Chiba

+81-43-226-2616

prc-jim@chiba-u.jp
Approval

none

History of Changes

No Publication date
6 April. 02, 2024 (this page) Changes
5 Mar. 27, 2024 Detail Changes
4 Dec. 27, 2023 Detail Changes
3 Aug. 08, 2023 Detail Changes
2 July. 31, 2023 Detail Changes
1 Jan. 11, 2022 Detail