Postoperative pain
Conditions
Interventions
postoperative acute phase (1-7 days) with low pain group:NA
Postoperative Acute Period (1-7 Days) High-Low Pain Group:NA
Postoperative Acute Period (1-7 Days) with persistent pain group:NA
Sponsors
Renji Hospital affiliated to Shanghai Jiaotong University School of Medicine
Eligibility
Sex/Gender
Female
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients who have pathological diagnosis of breast cancer and require surgical treatment; 2. Female patients aged 18 years or older; 3. Patients with an expected survival rate of more than 6 months; 4. Patients or their family member sign the informed consent form and they have good compliance.
Exclusion criteria
Exclusion criteria: 1. Patients who are unable to cooperate in completing information collection; 2. Patients with ASA grade of 3 or higher; 3. Patients who have had surgery within the past 6 months. 4. Patients who the researchers believe that are not suitable for this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The location, intensity, frequency and duration of the pain; | — |
Secondary
| Measure | Time frame |
|---|---|
| Neuropathic pain;Sudden, sharp pain;Level of anxiety;Severity of depression;The Effects of Pain on Sleep and Mood;Length of Stay for Patients;The time of opioid drug withdrawal;Unusual feeling;Adverse Drug Reactions;Complications from surgery and anesthesia.;Other postoperative analgesic measures; | — |
Countries
China
Contacts
Public ContactWeifeng Yu
Renji Hospital affiliated to Shanghai Jiaotong University School of Medicine
Outcome results
None listed