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Metabonomics study on immunotherapy of triple negative breast cancer with compound Sophora flavescens

Metabonomics study on immunotherapy of triple negative breast cancer with compound Sophora flavescens

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026982
Enrollment
Unknown
Registered
2019-10-27
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-10-28

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

Conditions

Triple negative breast cancer

Interventions

Triple negative breast cancer:matrine injection

Sponsors

The First Affiliated Hospital of Henan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) patients with tumor free survival of triple negative breast cancer; (2) patients aged 18-65 years (subject to the time of signing the informed consent); (3) patients who voluntarily participate in and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) patients with diabetes; (2) patients with other diseases under treatment; (3) patients with chemotherapy or radiotherapy less than 3 months; (4) patients with immune related drugs, radiation, nuclear medicine or surgery in the first three months; (5) patients with malignant tumors in the first five years (without complete cure of cervical carcinoma in situ, basal cells or squamous epithelial cells skin). Patients with cancer (6) received drug treatment within 7 days before admission. (7) during pregnancy and lactation; (8) those who have received blood transfusion of whole blood or component blood within 4 months; (9) those who are positive for any one of human immunodeficiency virus antibody, syphilis antibody and hepatitis C antibody; (10) those who are currently affected by intravenous transfusion and blood sampling diseases; (11) those who have participated in other clinical trials within 3 months before entering into the group; (12) those who are not considered suitable for entering the group or This test may not be completed for other reasons.

Design outcomes

Primary

MeasureTime frame
Serum metabolites;

Countries

China

Contacts

Public ContactShi Bingshuai

The First Affiliated Hospital of Henan University

sbs3766@163.com+86 13938613766

Outcome results

None listed

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