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A randomized controlled trial of Yanggan Yizhong Formula combined with standard treatment to improves survival in advanced gastric cancer

A randomized controlled trial of Yanggan Yizhong Formula combined with standard treatment to improves survival in advanced gastric cancer

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085753
Enrollment
Unknown
Registered
2024-06-18
Start date
2024-06-30
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Gastric cancer

Interventions

Experimental group:Traditional Chinese medicine And Standard treatment
Control group:placebo And Standard treatment

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Age 18-75 years old, gender is not limited; ?The diagnostic criteria of advanced gastric adenocarcinoma, and simultaneously met (1), (2) and (3) : (1) Stage IV; (2) Negative HER-2 gene test; (3) Immunohistochemical results were pMMR (MLH1+,PMS2+,MSH2+ and MSH6+). ? Meet the diagnostic criteria of Qixue deficiency syndrome. ? No antitumor therapy has been given since the diagnosis of advanced gastric cancer; ?ECOG score 0-2 points; ? Expected survival =3 months; ? Volunteer to join the study, sign the informed consent, and comply with the follow-up;

Exclusion criteria

Exclusion criteria: ? Patients with primary tumors of other sites; ? Treating patients who are or will participate in other clinical trials requiring intervention; ? Patients with severe, uncontrolled organic disease or infection, such as decompensated heart, lung and renal failure, resulting in inability to tolerate chemotherapy; ?Patients with a known allergy or intolerance to the investigational drug; ? Patients with mental illness; ? Pregnant or lactating patients.

Design outcomes

Primary

MeasureTime frame
Overall Survival;progression-free survival;

Secondary

MeasureTime frame
Objective Response Rate;QLQ-STO22;PG-SGA;

Countries

China

Contacts

Public ContactXue Peng

Wangjing Hospital, China Academy of Chinese Medical Sciences

xuepeng6399@163.com+86 131 2038 0194

Outcome results

None listed

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