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Effects of Thread Embedding Combined with Guided Surgery on Clinical Efficacy and Immune Function in Immunotherapy for Advanced Gastric Cancer

Effects of Thread Embedding Combined with Guided Surgery on Clinical Efficacy and Immune Function in Immunotherapy for Advanced Gastric Cancer

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122796
Enrollment
Unknown
Registered
2026-04-17
Start date
2026-04-17
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

gastric cancer

Interventions

Immunotherapy + Baduanjin group:Baduanjin
Immunotherapy:NA

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Age>= 18 years old, gender not limited; 2.Body weight > 45 kg; 3. Patients with advanced gastric malignant tumors, with clear pathological evidence; 4. Have not received systemic treatment before and are planned to receive first-line chemotherapy combined with immunotherapy; 5.ECOG score: 0-1, KPS score: 80-100; 6. Expected survival period >= 6 months; 7.Good compliance, voluntarily participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those with severe and uncontrolled organic lesions or infections, such as severe heart, lung or kidney failure, etc. 2.Those with severe psychological or physical functional disorders and unable to participate in physical exercise; 3. Those with brain trauma and intracranial hypertension; 4.The pain of the subjects is related to tumor emergencies such as intestinal obstruction/perforation, spinal cord compression, epidural metastasis or weight-bearing bone fractures or impending fractures; 5. Those with a history of autoimmune diseases; 6.Those with liver dysfunction (ALT >= 5×ULN, AST >= 5×ULN, TBIL>= 3×ULN) or kidney dysfunction (Cr>= 2.5×ULN); 7. Pregnant or lactating women; 8.Situations where the researcher deems the subject unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Cytokine Inflammation Index;Immunotherapy response rate: Complete Response (CR), Partial Response (PR), Stable Disease (SD), and Progressive Disease (PD).;Assessment scale;Survival analysis: overall survival (OS) and progression-free survival (PFS) within 2 years.;

Secondary

MeasureTime frame
Detection of transcription factors in gastric cancer tissue;Serum metabolomics analysis;Assessment of treatment-related toxicities and adverse reactions;

Countries

China

Contacts

Public ContactQing Li

Xuzhou Central Hospital

liqinglj@163.com+86 521 83956370

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026