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Efficacy and safety of AiYu capsule in combination with chemotherapy: the clinical trial in malignant lymphoma

Efficacy and safety of AiYu capsule in combination with chemotherapy: the clinical trial in malignant lymphoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006190
Enrollment
Unknown
Registered
2014-10-15
Start date
2015-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Malignant lymphoma

Interventions

Capsule group:Aiyu Capsule + The basic treatment of Western Medicine
control group:Kangsaidi+The basic treatment of Western Medicine

Sponsors

Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed as B-cell non-hodgkin's malignant lymphoma by imaging and/or histopathology or cytology; 2. The patients have clinically measurable focus, such as the enlargement of spleen or lymph node, nodular or tumorous; 3. In accordance with the standards of syndrome differentiation on deficiency of Qi and poison knot; 4. Aged between 18~75 years old, both gender; 5. The counts of leukocytes and platelets in recipient blood are in normal range (+/-20%); 6. The ALT values are over 2.5 times the upper normal limit, No serious diseases of heart, liver, kidney, blood and other systems; 7. performance status(KPS) score above 60 points;survival period is longer than 3 months; 8. Volunteers, and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients have mental diseases or cannot describe the syndromes clearly; 2. With the other severe internal diseases; 3. pregnant women and lactating women; 4. Not good medication compliance in previous treatment history; 5. Be allergic to the medicine in this research; 6. Patients are in the other clinical researches.

Design outcomes

Primary

MeasureTime frame
type-B ultrasonic;CT;MRI;

Secondary

MeasureTime frame
Hb;RBC;WBC;PLT;karnofsky;

Countries

China

Contacts

Public ContactXinyi Chen
chenxinyi0729@126.com+86 13601008250

Outcome results

None listed

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