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Multicenter clinical control study of noncytotoxic drug- gastric carcinoma D2 radical correction- Capecitabine combined therapy in gastric carcinoma

Clinical standard research of multicenter clinical control study of noncytotoxic drug- gastric carcinoma D2 radical correction- Capecitabine combined therapy in gastric carcinoma

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNRC-08000052
Enrollment
Unknown
Registered
2008-01-31
Start date
2008-02-01
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

Gastric carcinoma

Interventions

200mg, qod,5y Lanreotide 40mg, im, qm,2m
40mg, im, q6m,5y
6 cycles
combined group:Capecitabine 2500 mg/m2/d 2 w, resting 1 w
6 cycles. celecoxb afterward 400mg/d,2m
noncytotoxic drug taken group:celecoxb 400mg/d, 2m
200mg, qod, 5y Lanreotide 40mg, im, qm, 2m
40mg, im, q6m, 5y
chemotherapy group:Capecitabine 2500 mg/m2/d 2 w, resting1 w

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Gastric adenocarcinoma diagnosed by preoperative gastroscope and histopathology test; No peritoneal dissemination or out abdominal cavity metastasis observed by preoperative image analysis; Patients consent to accept gastric carcinoma radical correction aged between 18 and 70; Patients consent to accept preoperative noncytotoxic drug treatment and comment informed consent; Patients reselection on the basis of preoperative selection above mentioned. Postoperative including Criteria: Complete clinical and pathologic data, full registration in gastric carcinoma database; Lymph node scavenge scope D2, over 15 scavenged lymph node; Post operative pathologic diagnosis, staging, over 15 lymph node through pathologic test; Gastric carcinoma by postoperative pathologic diagnose; Willing to attend postoperative clinical research, to comment informed consent.

Exclusion criteria

Exclusion criteria: Preoperative excluding criteria: Drug allergy; Patients stand palliative and extenuative operation, expectant surgery or with remnant gastric cancer and concurrent malignant tumors from other origin;Pregnant women or expect gravidity in five years; Patients suffer from other severe diseases; Patients can not undertake follow-up visit; Postperative excluding criteria:Drug allergy; Less than 15 scavenged lymph node; Remote metastasis, peritoneal dissemination, ovaries metastasis, liver metastasis; Patients stand palliative and extenuative operation, expectant surgery, with out scavenged scope lymph node metastasis or with remnant gastric cancer and concurrent malignant tumors from other origin; Positive findings of exfoliative cytology in abdominal cavity;Stage I, IV gastric carcinoma by clinical pathologic diagnose; Patients can not undertake follow-up visit.

Design outcomes

Primary

MeasureTime frame
Survival rate;Regional and body recurrence rate;Quality of life;

Secondary

MeasureTime frame
Biochemical indicator, immune function,and other markers;

Countries

China

Contacts

Public ContactTang Cheng-Wei
cwtang@medmail.com.cn+86 028 81812275

Outcome results

None listed

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