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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05565027
Other study ID # 202101-02
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 20, 2022
Est. completion date October 20, 2023

Study information

Verified date September 2022
Source Shenzhen People's Hospital
Contact Jianyi Niu, MD
Phone +8617825846046
Email niujianyi001@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The digital X-ray system produced by Shenzhen Angell Technology Co., Ltd was selected as the tested equipment, and the powerlab biological signal acquisition and analysis system equipped with a pneumotachograph by ADInstruments was selected as the reference equipment. During the study, the lung volume measurements obtained by the lung function analysis method based on the dynamic digital radiography full respiratory cycle photography of the tested equipment was compared with the lung volume measurements obtained by the reference device pneumotachograph. The consistency of the lung volume measurements was used as the main validity evaluation index to observe the distribution of the differences between the measured values of the test device and the reference device, and to verify the validity of the declared product according to the main validity evaluation index.


Description:

Pulmonary function test is a test to explore the functional status of human respiratory system with the knowledge of exercise respiratory physiology and modern examination technology. It is an important test content for clinical diagnosis, severity assessment, treatment and prognosis assessment of chest and lung diseases, which has been widely used in the fields of respiratory medicine, surgery and anesthesiology. Compared with chest X-rays and CT examinations, which reflect the static function of the chest and lungs, pulmonary function tests can better reflect the dynamic functional changes of the body. However, pulmonary function test is not well performed to assess the functional status in patients with poor cooperation (e.g., poor lung function, inability to understand cooperation). Dynamic digital X-ray whole respiratory cycle photography uses advanced dynamic radiography and acquisition technology to obtain high-definition dynamic lung images during the whole respiratory cycle of the patient, and uses the industry's first rotating foot pedal to rotate the patient to obtain weighted 3D scan data and single-angle or multi-angle lung data. The patient's lung function is analyzed by algorithmically extracting the patient's full respiratory cycle airway nodes and branches and data statistics. For patients who cannot cooperate with the lung function, it can provid information on the dynamic function of the patient's chest and lungs for doctors to further improve clinical diagnosis and treatment. At present, the digital X-ray system (DTP580B-3) and the patient position fixation frame MRW-P1 manufactured by Shenzhen Angell Technology Co., Ltd. have passed the inspection by the inspection agency certified by the State Drug Administration of China (NMPA). Clinical trials were conducted to further evaluate the clinical effectiveness and safety of the products. The lung volume was measured using a pneumotachograph (with a physiological signal recorder) and a digital X-ray system (UC dynamic DR) in the same healthy subject, and the lung volume values measured by each of the reference device were analyzed for consistency to evaluate the validity of the lung volume measurement by the test device. And To evaluate the safety of the lung volume measurement function of the test device in clinical use based on the occurrence of device malfunctions, adverse events and serious adverse events in the trial.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date October 20, 2023
Est. primary completion date July 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: ? age = 18 years; ? subjects willing to undergo chest radiography; ? normal pulmonary ventilation function (forced vital capacity (FVC) = 80% of the expected value; forced expiratory volume in first second (FEV1) = 80% of the expected value; 1 second rate (FEV1/FVC) = 70%); ? can perform tidal breathing, deep inspiration and deep expiration; ? no history of smoking; ? no history of chronic respiratory disease; ? no acute respiratory disease within 4 weeks; ? subjects willing to provide written informed consent Exclusion Criteria: ? Pregnant and lactating women; ? Inability to stand alone; ? Severe vertigo and other adverse reactions to rotation in place.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Dynamic digital radiography
The use of advanced dynamic X-ray photography and acquisition technology can obtain high-definition dynamic lung images of patients throughout the respiratory cycle for analysis.
Pneumotachograph
The pneumotachograph monitors the flow rate, and the lung volume is calculated by integrating.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shenzhen People's Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Lung volume changes The volume of gas inhaled/exhaled during each respiratory session of the subject during the monitoring period. 1 day (The start time is when the subject is positioned and begins to breathe on command, and the end time is when the subject safely exits the x-ray system.)
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