Muscle Atrophy Clinical Trials

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Study on the Pathogenesis and Reversal Strategies of Cancer Cachexia Based on Multi-Omics

Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Cancer cachexia is a complex systemic metabolic syndrome with high incidence and mortality rates, significantly impacting the prognosis and survival of cancer patients.Current clinical comprehensive intervention approaches can only provide transient symptom relief and fail to fundamentally block or reverse muscle and fat loss. The core challenge lies in the extreme complexity of this pathological mechanism and the lack of early biomarkers.To overcome the limitations of traditional single-dimensional research approaches, this study proposes a combined analysis method utilizing multi-omics (imaging omics, pathological omics, metabolomics, and metagenomics) to construct a panoramic systemic model spanning macroscopic clinical manifestations and microscopic molecular processes. The aim is to comprehensively elucidate the pathogenesis and metabolic pathways of cachexia, thereby precisely identifying potential therapeutic targets capable of reversing this pathological process.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years

• Signed informed consent form and voluntary participation in this study

• Histologically and/or cytologically confirmed diagnosis of cancer

• Patients with gastrointestinal malignancies, including:

• Esophageal cancer

• Hepatocellular carcinoma

• Gastric cancer

• Cholangiocarcinoma

• Patients undergoing histopathological examination of primary lesion biopsy or gastrointestinal endoscopic biopsy

Locations
Other Locations
China
The First Affiliated Hospital of China Medical University
RECRUITING
Shenyang
Contact Information
Primary
Hanwen Liu
X18941960007@126.com
+86 18941960007
Backup
XiaoXu Liu
X18941960007@126.com
+86 18042901898
Time Frame
Start Date: 2026-03-18
Estimated Completion Date: 2028-03-20
Participants
Target number of participants: 1000
Treatments
Placebo_comparator: No nutritional intervention
No intervention was applied as a negative control to validate the experimental effect.
Active_comparator: Standard Nutritional Intervention
Standard intervention was administered as a positive control to validate experimental efficacy.
Active_comparator: Enhanced Nutritional Intervention
Validation of intervention efficacy through enhanced intervention in nutritionally high-risk patients
Related Therapeutic Areas
Sponsors
Leads: China Medical University, China

This content was sourced from clinicaltrials.gov