About this trial
Chronic postsurgical pain (CPSP) has an incidence of 46% in patients after breast cancer surgery, which seriously affects patients' physiological and psychological function, as well as quality of life. Acute pain is an independent risk factor for persistent pain after surgery. Erector spinae plane block (ESPB) provided excellent perioperative analgesia in patients undergoing breast surgery. Dexmedetomidine as an adjuvant of local anesthetics prolongs the duration of peripheral nerve block and decreases the requirements of postoperative analgesia. The investigators hypothesize that, for breast cancer patients undergoing mastectomy, ESPB (with a combination of 0.5% ropivacaine 35 ml and dexmedetomidine 1 microgram/kg) can reduce the occurrence of CPSP. The purpose of this randomized controlled trial is to investigate the impact of ESPB with adjuvant dexmedetomidine on the incidence of CPSP in breast cancer patients after mastectomy. We will also observe the impact of ESPB on long-term survival in these patients.
Eligibility criteria
Qualifiers
Age of 18 years or over, but less than 85 years;
Scheduled to undergo mastectomy for primary unilateral breast cancer.
Disqualifiers
Previous breast cancer surgery with an incision of >2 cm;
Chronic opioid dependence or long-term intake of analgesic medicines (>3 months);
Any contraindication to erector spinae plane block, including intrathoracic infection, infection at the puncture site, cancer invasion of the puncture site, severe spinal deformity, history of spinal surgery, and severe coagulopathy;
Inability to communicate in the preoperative period because of profound dementia, deafness, language barriers, or end-stage disease;
Trial design
Treatments tested in this trial
- Erector spinae plane block
- Control group
Treatment groups
Sponsors and collaborators
Peking University First Hospital
Lead sponsor
Peking University Cancer Hospital & Institute
Collaborator