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Effect of regional block on chronic pain after breast cancer surgery and establishment of chronic pain prediction model based on NLRP3 inflammasome signal pathway

Effect of regional block on chronic pain after breast cancer surgery and establishment of chronic pain prediction model based on NLRP3 inflammasome signal pathway

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064439
Enrollment
Unknown
Registered
2022-10-08
Start date
2022-10-15
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Breast Cancer

Interventions

group A:General anesthesia of Sevoflurane
group B:General anesthesia of Sevoflurane+paravertebral nerve block(PVB)
group C:General anesthesia of Sevoflurane+pectoral nerves block-?(PECS-?)

Sponsors

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who voluntarily participated in the study and signed written informed consent; 2. Female aged 18-70 years at the time of signing the informed consent; 3. Histological or cytological confirmation of breast adenocarcinoma; 4. Surgical treatment under elective general anesthesia is proposed; 5. American society of anesthesiologists (ASA) grades ?-?.

Exclusion criteria

Exclusion criteria: 1. Patients with inflammatory diseases; 2. Patients who received surgical treatment within the last 30 days; 3. Pregnant patients; 4. Patients with kidney disease; 5. Long-term use of sedatives or antidepressants and other psychotropic drugs; 6. Contraindicated regional nerve block; 7. Difficulties in language comprehension, mental illness, inability to visit hospitals for follow-up visits, etc.; 8. Taking other investigational drugs or participating in other clinical trials within the 3 months prior to study inclusion; 9. Preoperative radiotherapy or chemotherapy; 10. Other conditions not considered suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
postoperative chronic pain within 3 months;

Secondary

MeasureTime frame
explore the analgesic effects of different blocking techniques under different degrees of surgical trauma;compare the expression of ASC, pro-caspase-1, caspase-1 and IL-1ß & IL-18 in NLRP3 inflammasome signal pathway in peripheral blood monocytes before/or 1 day after operation;explore the effect of pain on tumor prognosis;establishment and validation of CPSP prediction model for breast cancer;postoperative serum expression of NLRP3 inflammasome in peripheral blood monocytes;

Countries

China

Contacts

Public ContactYan Tao

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

blizzardyt@163.com+86 13522553375

Outcome results

None listed

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