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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05933317
Other study ID # 202212301
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date December 31, 2024

Study information

Verified date July 2023
Source Beijing Chao Yang Hospital
Contact Tao Ouyang, Dr.
Phone +86 18720931226
Email ouyt1996@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

So far, the number of COVID-19 infections worldwide has exceeded 700 million. Long-term damage to the lungs is a major sequela of COVID infection. Pulmonary function testing is an important means for the evaluation of lung damage. MRI examinations with free breathing and no contrast agent can prevent patients from suffering from ionizing radiation damage caused by multiple CT examinations.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date December 31, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Older than 18 years; Sign the informed consent; Patients diagnosed with COVID-19 by nucleic acid test and survived to be discharged; Complete clinical data during hospitalization. Exclusion Criteria: - Patients with bacterial pneumonia; Patients with MRI contraindications.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Functional lung MRI
Functional lung MRI

Locations

Country Name City State
China Beijing Chaoyang Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Chao Yang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary QDP, VDP perfusion defect percentage, ventilation defect percentage 6 months
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