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Preventive and therapeutic effects of probiotics on skin and mucosal reactions induced by liposome doxorubicin chemotherapy in breast cancer patients: a randomized controlled study

Preventive and therapeutic effects of probiotics on skin and mucosal reactions induced by liposome doxorubicin chemotherapy in breast cancer patients: a randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024927
Enrollment
Unknown
Registered
2019-08-03
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Breast Cancer

Interventions

placebos group:placebos

Sponsors

The Third Xiangya Hosipital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed breast cancer patients undergoing chemotherapy with liposome-containing doxorubicin regimen; 2. Aged 20 to 60 years; 3. No disease of immune system; 4. Agree to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Suffer from skin diseases such as intractable oral ulcer, psoriasis, eczema, tinea manus and pedis, and other diseases (such as syphilis) that may cause skin damage; 2. Patients with diabetes, impaired glucose tolerance and lactose intolerance; 3. Patients with coronary heart disease, myocardial infarction and poor cardiac function; 4. Patients with extreme organ failure and severe immunosuppression; 5. Participating in other clinical trials; 6. Patients with serious liver and kidney diseases; 7. Have dementia (defined as MMSE score = 2 points) or Parkinson's disease or other neurological diseases causing dysfunction, as well as the history of brain injury, cerebral hemorrhage, stroke, brain tumor, cerebral infarction and other diseases; 8. Advanced patients or patients with other malignant tumors; 9. Having mental illness or family history of mental illness; 10. Alcoholic or drug addicts; 11. Those who refuse to join the group and cannot cooperate with the treatment; 12. In the opinion of the attending physician or researcher, there are other circumstances that are not suitable for the study.

Design outcomes

Primary

MeasureTime frame
Toxicity of oral, hand, foot and skin mucosa;

Countries

China

Contacts

Public ContactTong Jianbin

The Third Xiangya Hosipital, Central South University

498836726@qq.com+86 15386429820

Outcome results

None listed

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