Skip to content

Feasibility Study of Phase-Resolved Functional Lung (PREFUL) MRI for Quantitative Assessment of Pulmonary Function in Healthy Volunteers

Feasibility Study of Phase-Resolved Functional Lung (PREFUL) MRI for Quantitative Assessment of Pulmonary Function in Healthy Volunteers

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116547
Enrollment
Unknown
Registered
2026-01-12
Start date
2025-03-22
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Magnetic Resonance Imaging

Interventions

Index test:Phase-Resolved Functional Lung (PREFUL) MRI

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Subject eligibility will be met if one of the following criteria is fulfilled: For Healthy Volunteers: (1) Age >= 18 years; (2) In good health with no history of cardiovascular or pulmonary diseases; (3)Non-smoker or smoking history of less than 1 pack-year; (4)No upper respiratory tract infection within the past 4 weeks. For Patients with Respiratory System Diseases: (1) Age >=18 years; (2) Diagnosis of a respiratory system disease, such as pneumonia, pulmonary tuberculosis, asthma, chronic obstructive pulmonary disease, bronchiectasis, pulmonary embolism, pulmonary fibrosis, lung cancer, etc.

Exclusion criteria

Exclusion criteria: 1.For Healthy Volunteers: (1) Contraindications to magnetic resonance imaging (e.g., presence of metallic implants, claustrophobia, pregnancy); (2)Smoking on the day of the examination; (3)Contraindications to conventional pulmonary function tests (e.g., history of temporomandibular joint dislocation, having undergone endoscopy and biopsy on the same day, poor cooperation, or physically debilitated patients). 2.For Patients with Respiratory System Diseases: Contraindications to magnetic resonance imaging (e.g., presence of metallic implants, claustrophobia, pregnancy).

Design outcomes

Primary

MeasureTime frame
Ventilation defect percentage;Flow-volume loop correlation coefficient;Perfusion defect percentage;Perfusion quantified;

Secondary

MeasureTime frame
Regional ventilation;Ventilation/perfusion matching-related indices;

Countries

China

Contacts

Public ContactChunchao Xia

West China Hospital, Sichuan University

xiachunchao@wchscu.cn+86 189 8060 6885

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026