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Clinical Trials in China / NCT06327594
Recruiting Observational

Assessment System of Sarcopenia in Lung Cancer Patients

NCT06327594 · tracked via the Priya Life Science China tracker
Sponsor
West China Hospital
Phase
Observational
Started
2023-11-01
Last updated
2024-03-25

Condition(s) studied

SarcopeniaLung CancerUltrasound

Investigational drug(s) / intervention(s)

ultrasound scanCT/MRI scan

ultrasound scan: The patients with lung cancer who are scheduled to undergo radical resection of lung cancer are examined by ultrasound at multiple sites of the whole body, including muscle and fat.

CT/MRI scan: The patients with lung cancer who are scheduled to undergo radical resection of lung cancer are examined by abdominal CT/MRI.

Study summary

1. To explore the diagnostic value of musculoskeletal cross-modal imaging assessment system of ultrasound combined with abdominal CT/MRI for sarcopenia in patients with lung cancer.
2. To explore the value of musculoskeletal cross-modal imaging assessment system of ultrasound combined with abdominal CT/MRI in evaluating the prognosis and the effect of nutritional support in patients with lung cancer during perioperative period.
3. To explore the value of musculoskeletal cross-modal imaging assessment system of ultrasound combined with abdominal CT/MRI in evaluating the long-term prognosis of patients with lung cancer.

Eligibility

Sex
ALL
Min age
40 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: 1. Hospitalized patients scheduled for radical resection of lung cancer. 2. With a CT/MRI examination within 1 week. 3. The compliance of examination was good. Exclusion Criteria: 1. Amputated arm or leg. 2. Severe oedema (oedema higher than knee level). 3. Implantable pacemaker. 4. Impaired consciousness, poor general health, or other reasons that would prevent the individual from completing the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Xinyi Tang Chengdu Sichuan Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06327594 on ClinicalTrials.gov ↗ ← All trials in China