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Effects of anesthesia techniques on postoperative inflammatory response, pain and prognosis in patients with breast cancer

Effects of anesthesia techniques on postoperative inflammatory response, pain and prognosis in patients with breast cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038627
Enrollment
Unknown
Registered
2020-09-26
Start date
2020-10-20
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Breast cancer

Interventions

TIVA group:Total intravenous anesthesia was used (breast conserving subgroup n = 20, simple mastectomy subgroup n = 20)
SEV group:Sevoflurane inhalation anesthesia was used (breast conserving subgroup n = 20, simple mastectomy subgroup n = 20)
PVB+general group:aravertebral block combined with general anesthesia (breast conserving subgroup n = 20, simple mastectomy subgroup n = 20)
general group:General anesthesia was used (breast conserving subgroup n = 20, simple mastectomy subgroup n = 20)

Sponsors

Shenzhen Hospital, cancer hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients who voluntarily participated in the study and signed a written informed consent; 2. Aged 18 to 60 years old; 3. Histology or cytology confirmed breast adenocarcinoma; 4. The operation of unilateral breast cancer under general anesthesia is proposed; 5. The American Society of Anesthesiology (ASA) was graded grade I or II; 6. Asian race.

Exclusion criteria

Exclusion criteria: 1. Patients with inflammatory diseases; 2. Patients who received surgical treatment in the last 30 days; 3. Pregnant women; 4. Patients with hepatorenal diseases 5. Long term drinking, long-term use of sedative drugs or antidepressants and other mental drugs; 6. There are contraindications of paravertebral nerve block, including severe abnormal coagulation function, infection of puncture site, trauma or spinal operation history; 7. For any reason, the study can not be cooperated with, such as: language understanding difficulties, mental illness, inability to visit hospital for follow-up, etc; 8. Take other trial drugs or participate in other clinical trials within 3 months before the study was selected; 9. Before operation, they were treated with radiotherapy or chemotherapy; 10. The researchers believe that it is not suitable to be included in other cases of this experiment.

Design outcomes

Primary

MeasureTime frame
NLRP3;ASC;pro-caspase-1;caspase-1;IL-1ß;IL-18;pain;Disease free survival;Overall survival;

Countries

China

Contacts

Public ContactSun Li

Shenzhen Hospital, cancer hospital, Chinese Academy of Medical Sciences

ykyzlyysunli@126.com+86 13801231361

Outcome results

None listed

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