Apatinib for Resectable Colorectal Cancer
- Sponsor
- Nanchong Central Hospital
- Study ID
- NCT03228043
- Status
- Withdrawn
Conditions
- Adjuvant Chemotherapy
- Apatinib
- Colorectal Cancer
- Outcome, Fatal
- Surgery
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib — DRUGApatinib combine with CAPEOX adjuvant chemotherapy for resectable colorectal
- CAPEOX — DRUGCAPEOX adjuvant chemotherapy for resectable colorectal
Study Details
Objective: To compare the outcome of patients with colorectal cancer who treated with adjuvant therapy or Apatinib with adjuvant therapy postoperatively. Language: English.
Key Dates
- Start date
- Mar 1, 2020
- Status verified
- Nov 2024
- Primary completion
- Mar 1, 2021
- Completion
- Mar 1, 2023
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Apatinib groupApatinib combined with CAPEOX program. Apatinib tablets: 500 mg po qd from the second cycle of chemotherapy. Oxaliplatin: Day 1, 130mg/m2, IV infusion. Capecitabine: Day 1-14, 1000mg/m2 Twice Daily, po. A total of 6 cycles, 3 weeks apart of chemotherapy.
- Placebo Comparator: Control groupCAPEOX program. Oxaliplatin: Day 1, 130mg/m2, IV infusion. Capecitabine: Day 1-14, 1000mg/m2 Twice Daily, po. A total of 6 cycles, 3 weeks apart of chemotherapy.
Primary Outcome Measure
Number of Participants recurrence-free survival [ Time Frame: 1 year ]
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