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The reverse effect of Asipirin on oxaliplatin-resistant patients

Aspirin and FOLFOX in Previously Treated Patients With Metastatic Colorectal Cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-12001907
Enrollment
Unknown
Registered
2012-02-03
Start date
2009-01-03
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Advanced chemoresistant colorectal cancer

Interventions

trial group:Aspirin + FOLFOX4

Sponsors

The Fourth Affiliated Hospital, Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
26 Years to 72 Years

Inclusion criteria

Inclusion criteria: Eligible patients had histologically proven metastatic colorectal adenocarcinoma with documented progressive disease after first-line and second-line chemotherapy. Patients developing metastatic disease within 6 months of receiving adjuvant therapy were also included. Other criteria for eligibility included measurable disease by Response Evaluation Criteria in Solid Tumors Group criteria, had a period of at least 4 weeks since their last round of chemotherapy, had an Eastern Cooperative Oncology Group (ECOG) performance status of 2 or less. Laboratory criteria include WBC count>=3.5*10^9/L, neutrophil count>=1.5*10^9/L, platelet count >=100*10^9/L, haemoglobin level>=9g/dL, serum bilirubin level<=2.0mg/dL, serum AST/ALT and alkaline phosphatase level<=2 times the upper limit of normal, the serum creatinine level <=1.5mg/dL.

Exclusion criteria

Exclusion criteria: aspirin hypersensitivity, digestive ulcer or active bleeding patients.

Design outcomes

Primary

MeasureTime frame
effect rate;

Countries

China

Contacts

Public ContactShujian Chang
changsj88265@sina.com+86 15312238773

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026