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Clinical study on the prevention and treatment of tumor chemotherapy-induced gastrointestinal reactions by Jianpi Yiwei Decoction

Clinical study on the prevention and treatment of tumor chemotherapy-induced gastrointestinal reactions by Jianpi Yiwei Decoction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092390
Enrollment
Unknown
Registered
2024-11-15
Start date
2024-09-06
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

tumor chemotherapy-induced gastrointestinal reactions

Interventions

Experimental group:Conventional antiemetic therapy+ Yiwei formula
Control group:Conventional antiemetic therapy+Jianpi Yiwei Formula placebo (1/10 Jianpi Yiwei Formula)

Sponsors

Cancer Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients who have not previously undergone chemotherapy; (2) Aged between 18 and 80 years; (3) Diagnosed with non-small cell lung cancer via pathological examination; (4) Individuals of all genders intending to receive two or more cycles of carboplatin-based chemotherapy (administered every 21 or 28 days); (5) Karnofsky Performance Status (KPS) score of 70 or above.

Exclusion criteria

Exclusion criteria: (1) Presence of unstable brain metastases; (2) Planned to receive or have received epigastric or cranial radiotherapy within the past four weeks; (3) History of major gastrointestinal surgery (such as cholecystectomy, significant intestinal resection, or gastrectomy) within the last five years; (4) A documented history of chronic gastrointestinal diseases (including ulcerative colitis and Crohn's disease) assessed for potential impact; (5) Evidence of gastrointestinal bleeding; (6) A history of substance abuse, including drugs or alcohol; (7) Any relevant circumstances that may compromise the evaluation of the study; (8) Known allergies to any components in the Jianpi Yiwei prescription.

Design outcomes

Primary

MeasureTime frame
Complete Control rate;

Secondary

MeasureTime frame
The impact of nausea and vomiting on daily life;Control rate to anorexia;The impact of fatigue on daily life;Stool situation;Control rate to bloating;

Countries

China

Contacts

Public ContactLi Feng

Cancer Hospital, Chinese Academy of Medical Sciences

fengli663@126.com+86 186 1814 7576

Outcome results

None listed

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