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Clinical Trials in China / NCT06606912
Active, not recruiting Observational

Predictive Effect of Abdominal Fat and Muscle Area Calculated Based on Abdominal CT on Gastric Cancer Patients

NCT06606912 · tracked via the Priya Life Science China tracker
Sponsor
First Affiliated Hospital of Chongqing Medical University
Phase
Observational
Started
2012-01-01
Last updated
2024-09-23

Condition(s) studied

Gastric CancersColorectal CancerSarcopeniaObesity and Overweight

Investigational drug(s) / intervention(s)

Skeletal muscle, subcutaneous fat and visceral fat area

Skeletal muscle, subcutaneous fat and visceral fat area: CT-based measurement of skeletal muscle, subcutaneous fat and visceral fat areas at L1, L2, L3, L4 and L5 levels.

Study summary

This study aims to create a clinical prediction model. Abdominal fat and muscle area also play an important role in the prediction of surgical outcomes in colorectal cancer. Studies have shown that excess visceral fat and low skeletal muscle mass (sarcopenia) are associated with poorer postoperative outcomes, including a higher risk of postoperative complications and lower survival. Preoperative imaging techniques such as CT, MRI and ultrasound that provide accurate measurements to assess abdominal fat and muscle area can help surgeons develop individualized surgical and rehabilitation plans, improve surgical success, reduce complications and improve long-term patient prognosis. In this study, the investigators expected to construct a prediction model of abdominal fat and muscle area on the short- and long-term outcomes of gastric and colorectal cancer patients by calculating the abdominal fat and muscle area in different levels of abdominal CT images, in order to further adjust and guide the treatment plan.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Diagnosis of gastric cancer or colorectal cancer confirmed by pathology or cytology; 2. aged \>18 years; 3. not received chemotherapy, radiotherapy, targeted therapy or immunotherapy; 4. post-operative pathological stages other than stage IV, or no liver, lung or other organs as confirmed by CT, MRI, B-ultrasound imaging. 5. patients who have pre-operative CT examination data kept in our hospital. Exclusion Criteria: 1. Poor quality of preoperative CT images; 2. refusal to participate in this study.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
the First Affiliated Hospital of Chongqing Medical University Chongqing Chongqing Municipality
the Second Affiliated Hospital of Chongqing Medical University Chongqing Chongqing Municipality
The Affiliated Yongchuan Hospital of Chongqing Medical University Chongqing Chongqing Municipality

More First Affiliated Hospital of Chongqing Medical University trials in China

Other trials for the same condition

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 NCT06606912 on ClinicalTrials.gov ↗ ← All trials in China