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Study on the consistency of left diaphragm displacement in rehabilitation patients using multiple ultrasound alternative measurement methods

Study on the consistency of left diaphragm displacement in rehabilitation patients using multiple ultrasound alternative measurement methods

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105835
Enrollment
Unknown
Registered
2025-07-11
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Weakened diaphragm

Interventions

Observation group:None
Control group:None

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Observation group: (1) Age >= 18 years old; (2) Patients with weakened muscle strength in at least one limb who are hospitalized for treatment in the rehabilitation department; (3) No obvious abnormal lung diseases were found through pulmonary CT, chest X-ray or pulmonary ultrasound examination; (4) Regularly undergo ultrasound examination and voluntarily participate in the study, cooperate with the examiner to complete diaphragmatic ultrasound examination, and obtain informed consent. 2.Control group: (1) Age >= 18 years old; (2) Good limb muscle strength and motor function; (3) Healthy individuals with heart, lung, and diaphragm related diseases; (4) Voluntarily participate in the study and cooperate with the examiner to complete the diaphragmatic ultrasound examination, and obtain informed consent.

Exclusion criteria

Exclusion criteria: 1.Observation group: (1) Respiratory center related diseases and neuromuscular conduction disorders related diseases; (2) History of lung, mediastinal, or abdominal surgery; (3) Lung, mediastinal or diaphragmatic tumors; (4) Pregnant women, spinal or chest wall deformities, etc; (5) Unable to obtain clear ultrasound images or other factors unsuitable for inclusion in the study; (6) Currently participating in other intervention studies. 2.Control group: (1) Patients with chest, lung, mediastinal, or respiratory center related diseases; (2) The subjects are unable to cooperate in completing the study, unable to obtain clear ultrasound images, or other factors that are not suitable for inclusion in the study; (3) I am currently participating in other intervention studies.

Design outcomes

Primary

MeasureTime frame
Diaphragm displacement;Renal displacement;Pleural sliding displacement;Alternative position of diaphragm displacement;Splenic displacement;

Countries

China

Contacts

Public ContactZhao Haotian

Hebei General Hospital

1011192637@qq.com+86 311 85989973

Outcome results

None listed

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