Skip to content

A randomized controlled trial for intra-arterial infusion chemotherapy combined with sodium bicarbonate and systemic chemotherapy for unresectable gastric cancer

A randomized controlled trial for intra-arterial infusion chemotherapy combined with sodium bicarbonate and systemic chemotherapy for unresectable gastric cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020701
Enrollment
Unknown
Registered
2019-01-14
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

gastric cancer

Interventions

Group 1:Systemic chemotherapy plus oral chemotherapy group
Group 2:Arterial catheter infusion chemotherapy plus oral chemotherapy
Group 3:Arterial catheter infusion chemotherapy + oral chemotherapy + sodium bicarbonate

Sponsors

The Second affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients aged 18 to 75 years; 2) Ultrasound gastroscopy or imaging (CT) can diagnose potentially unresectable gastric cancer (T4a-bN2-3M0) with indications of neoadjuvant chemotherapy or transformation therapy; 3) Pathological diagnosis of gastric cancer; 4) No contraindication of chemotherapy; 5) Patients who did not undergo chemotherapy or were diagnosed for the first time.

Exclusion criteria

Exclusion criteria: 1) Those who fail to comply with the requirements of the trial, obviously violate this regimen, or change to other regimens in the course of treatment; 2) The life expectancy of patients with extensive systemic metastasis is less than 3 months; 3) Leukocyte count is less than 2*109/L and platelet count is less than 75*10^9/L; 4) Severe heart, liver and kidney diseases, unable to tolerate chemotherapy; 5) Patients without gastric cancer complications such as massive gastrointestinal bleeding and perforation need to be treated in emergency department; 6) Patients with distant metastasis (excluding group 16 lymph node metastasis); 7) Patients with other tumors, with a history of malignant tumors (excluding early primary cancers); 8) The patient himself asked to withdraw from the trial; 9) Researchers believe that patients are not suitable for this study.

Design outcomes

Primary

MeasureTime frame
Successful conversion rate of operation;

Secondary

MeasureTime frame
ORR;PFS;

Countries

China

Contacts

Public ContactMing Chao

The Second affiliated Hospital, Zhejiang University School of Medicine

z2doctor_chaoming@163.com+86 13957139239

Outcome results

None listed

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