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A prospective, randomized, controlled, multicenter clinical study on the intervention of indolent lymphoma with the "Jieduxiaoluo Formula"

A prospective, randomized, controlled, multicenter clinical study on the intervention of indolent lymphoma with the "Jieduxiaoluo Formula"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000851
Enrollment
Unknown
Registered
2026-04-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Indolent Lymphoma

Interventions

Treatment group:Differential Diagnosis and Treatment Based on Typology

Sponsors

The First Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: I. Age range: 18 - 80 years old, gender not restricted. Before inclusion, informed consent must be signed; II. According to the NCCN 2024 guidelines, the diagnosis through histopathology is clear: chronic lymphocytic leukemia / small B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, and patients who can undergo observation and waiting; III. There are measurable and assessable lesions for efficacy evaluation, and the expected survival period is more than 4 months.

Exclusion criteria

Exclusion criteria: I. Pregnant or lactating women, or those planning pregnancy during treatment or unable to take effective contraceptive measures; II. Severe immunodeficiency, or active infection, or coexisting other autoimmune diseases such as SLE, RA, etc.; III. Uncontrolled hypertension or diabetes; IV. Significantly abnormal liver or kidney function; V. Positive serum HIV or HCV test results, or HBV in active stage; VI. Patients with poor compliance; VII. Any other situation that the researcher deems inappropriate for participation in this study.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Progression-free survival;Cytokine;Lymphocyte subsets;Genetic fragment variation;Hotspot gene mutations;Chromosome karyotype;

Countries

China

Contacts

Public ContactBaodong Ye

The First Affiliated Hospital of Zhejiang Chinese Medical University

13588453501@163.com+8613588453501

Outcome results

None listed

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