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Construction of a Spatiotemporal Omics Database for TCM Syndromes Based on Multidimensional Efficacy Evaluation in Patients Receiving Targeted Therapy for Colorectal Cancer

Construction of a Spatiotemporal Omics Database for TCM Syndromes Based on Multidimensional Efficacy Evaluation in Patients Receiving Targeted Therapy for Colorectal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026000609
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-03-20
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Colorectal cancer

Interventions

Bevacizumab group:Standard late-stage first-line postoperative adjuvant chemotherapy

Sponsors

Ethics Committee of the Second Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Pathologically confirmed as stage IV metastatic colorectal cancer; (2) Planned to receive initial treatment with FOLFIRI/FOLFOX combined with bevacizumab/cetuximab; (3) Age =18 years; (4) Expected survival =3 months; (5) Normal cognitive function and able to cooperate with the study; (6) Signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Severe gastrointestinal diseases (e.g., intestinal perforation infection, Crohn's disease, ulcerative colitis) or autoimmune diseases; (2) Severe cardiovascular diseases (e.g., myocardial infarction, heart failure (NYHA III–IV class), stroke, uncontrolled hypertension (systolic blood pressure =180 mmHg and/or diastolic blood pressure =110 mmHg), etc.), liver or kidney failure, or hematological diseases; (3) History of drug or alcohol abuse; (4) Pregnancy or breastfeeding; (5) Use of antibiotics or probiotic formulations within 2 weeks prior to treatment; (6) Participation in other drug clinical trials within the past 3 months; (7) Planned radiotherapy; (8) Assessed by the investigator as unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
progression-free survival;

Secondary

MeasureTime frame
overall survival;Colorectal Surgical Tissue Sections Omics Analysis;Blood Metabolomics, Genomics, Proteomics;

Countries

China

Contacts

Public ContactYAO Qinghua

The Second Affiliated Hospital of Zhejiang Chinese Medical University, Xinhua Hospital of Zhejiang Province

20234052@zcmu.edu.cn13588899111

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026