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Comparison of the effects of seed-containing and seedless auricular pressure therapy in treating chemotherapy-related diarrhea in patients with spleen and stomach deficiency syndrome of colorectal cancer

Comparison of the effects of seed-containing and seedless auricular pressure therapy in treating chemotherapy-related diarrhea in patients with spleen and stomach deficiency syndrome of colorectal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119028
Enrollment
Unknown
Registered
2026-02-14
Start date
2026-02-18
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Chemotherapy-related diarrhea in colorectal cancer

Interventions

Control group:Conventional basic internal medicine nursing treatment + Auricular acupressure (seedless)
Experimental group:Internal medicine routine care + Auricular point pressing (with seeds)

Sponsors

The First Affiliated Hospital of Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 80 years old, gender and ethnicity are not restricted; 2. Meet the Western medical diagnosis criteria for colorectal cancer; 3.Patients with colorectal cancer who are currently undergoing chemotherapy regimens containing irinotecan or 5-Fu; 4.Meet the diagnostic criteria for diarrhea and syndromes in both traditional Chinese and Western medicine after using chemotherapy drugs,before chemotherapy, defecation was normal, and there was no habitual diarrhea; 5.Diarrhea grade is 1-3; 6.Karnofsky Performance Status Score (KPS) >= 60 points; 7. Ear is intact without injury, no scars, not allergic to alcohol and tape, and suitable for auricular acupressure; 8. Conscious, voluntarily participating in this study, and signing the informed consent form. Note: Only patients meeting all 8 criteria can be included in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with diarrhea caused by other diseases;patients who have been taking drugs that affect intestinal function for a long time; 2. Patients with severe primary diseases such as cardiovascular diseases (unstable angina pectoris, severe arrhythmia, myocardial infarction within 6 months), liver diseases (acute renal failure, grade C liver cirrhosis), kidney diseases (chronic renal failure), digestive tract diseases (active gastrointestinal bleeding, acute phase of inflammatory bowel disease, intestinal obstruction), or other tumors; 3.Lactating women or those planning to get pregnant within the next three months; 4. Patients currently participating in or recently participating in other studies; 5. Patients with inflammation, eczema, ulcers, frostbite or large scar tissue on the ear skin; 6.Patients with severe infections. Note: All patients meeting any of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
Daily frequency of defecation;

Secondary

MeasureTime frame
Quality of life score;Traditional Chinese Medicine Symptom Score;Adverse Event Assessment Questionnaire;Grading of stool characteristics;

Countries

China

Contacts

Public ContactChen Lingxuan

The First Affiliated Hospital of Xiamen University

150072373@qq.com+86 10 12345678

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026