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A Study on the Prognosis of Breast Cancer Surgery Patients Based on the Mitochondrial Mass and Mitochondrial Membrane Potential of Immune Cells and Tumor Cells

A Study on the Prognosis of Breast Cancer Surgery Patients Based on the Mitochondrial Mass and Mitochondrial Membrane Potential of Immune Cells and Tumor Cells

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099749
Enrollment
Unknown
Registered
2025-03-27
Start date
2024-06-13
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Breast Cancer

Interventions

Group of breast cancer:None
Group of benign breast tumors:None

Sponsors

Shaoxing Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All breast cancer patients (Stage I to Stage III) who meet the inclusion criteria, as well as patients with benign breast lesions undergoing surgical treatment, will be included. Breast cancer patients will undergo diagnostic staging within four weeks before the start of treatment; metastatic lesions will be excluded during the initial diagnostic staging. Specific inclusion criteria should refer to the "relevant clinical guidelines".

Exclusion criteria

Exclusion criteria: 1.Previously received any form of immunotherapy; 2.Diagnosed with or treated for malignancies other than breast cancer; 3.Presence of any active autoimmune disease or history of such; 4.Patients with uncontrolled diabetes; 5.Pregnant or lactating women; 6.Duplicate peripheral blood samples collected from the same subject at different time points; 7.Peripheral blood samples with unclear sample type, sample collection time, or case information; 8.Peripheral blood samples contaminated due to experimental operations or samples with insufficient quantity for testing; 9.Peripheral blood samples that do not meet storage conditions; 10.Subject samples collected at time points not in accordance with the protocol requirements; 11.Subjects with neurodegenerative or psychiatric disorders.

Design outcomes

Primary

MeasureTime frame
MitoDye,Mitochondria-specific markers;

Countries

China

Contacts

Public ContactGuodong Ruan

Shaoxing Second Hospital

recardos@163.com+86 137 5757 9991

Outcome results

None listed

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