|
Feasibility Study of Deep Learning-based MDixon Quant for Quantitative Assessment of Chemotherapy-induced Fatty Liver
RECRUITINGN/ASponsored by Yunnan Cancer Hospital
Actively Recruiting
PhaseN/A
SponsorYunnan Cancer Hospital
Started2023-12-25
Est. completion2024-12-30
Eligibility
Age18 Years – 80 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06735118
Summary
The purpose of this study is to quantitatively assess the changes in liver fat content in cancer patients before and after treatment. The main questions it aims to answer are:How does the liver fat fraction change before and after chemotherapy? In this study, patients undergoing mDixon Quant scanning are subjected to fully automated segmentation and measurement of liver fat content using artificial intelligence.
Eligibility
Age: 18 Years – 80 YearsHealthy volunteers accepted
Inclusion Criteria: 1. CT/B ultrasound showed no fatty liver 2. No MRI contraindications, including pacemaker, stent, metal implant, or claustrophobia 3. Received neoadjuvant/adjuvant chemotherapy Exclusion Criteria: 1. Missing follow-up information 2. Liver lesions (metastases, hemangioma, etc.) 3. Poor image quality
Conditions2
Liver DiseaseNon Alcoholic Fatty Liver Disease
Interventions1
Related trials
- AI Prediction of Gastric Cancer Response to Neoadjuvant Chemotherapy — Chinese Academy of Sciences
- Effect of Neoadjuvant Chemotherapy on MRI Accuracy Before Cystectomy — Assiut University
- Iparomlimab and Tuvonralimab Combined With Paclitaxel and Cisplatin as Neoadjuvant Therapy for CC — Obstetrics & Gynecology Hospital of Fudan University
- Neoadjuvant Chemotherapy for Locally Advanced Gall Bladder Cancer : a Randomized Control Trial (NEOGB) — Rajiv Gandhi Cancer Institute & Research Center, India
- Neoadjuvant Chemotherapy for Obstructive Colon cancER First Treated by cOlostomy — University Hospital, Rouen
- Neoadjuvant Chemotherapy in Combination With Toripalimab for HR+/HER2- Breast Cancer : a Randomized, Open-label, Parallel-controlled, Multi-center Phase III Study (NEOTORCH-BREAST04) — First Affiliated Hospital of Zhejiang University
- Neoadjuvant SBRT Followed by Nab-Paclitaxel Combined With Toripalimab in HR+/HER2- Breast Cancer — Xijing Hospital
- Neoadjuvant Therapy Combined With Trastuzumab Rezetecan and Toripalimab for HR+/HER2-low Breast Cancer (NEOTORCH-BREAST 08) — First Affiliated Hospital of Zhejiang University
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
Actively Recruiting
PhaseN/A
SponsorYunnan Cancer Hospital
Started2023-12-25
Est. completion2024-12-30
Eligibility
Age18 Years – 80 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06735118