Analysis of the Incidence and Risk Factors of Chronic Pain After Cesarean Section
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-50
SponsorHuazhong University of Science and Technology
About this trial
Persistent postoperative pain is a globally recognized issue that deserves attention. Cesarean section is one of the surgeries that may cause persistent postoperative pain. PSPP may affect communication between mother and baby, and may lead to postpartum depression, which has a negative impact on the daily activities and quality of life of mothers. It is an important clinical issue.
The main purpose of this study is to (1) prospectively investigate the overall incidence and characteristics of persistent pain after cesarean section at 3, 6, and 12 months after surgery; (2) Use regression analysis and data modeling analysis to evaluate the relationship between perioperative variables and chronic pain in postpartum women undergoing cesarean section; (3) Analyze the relationship between chronic pain after cesarean section and postpartum depression in postpartum women.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age range from 20 to 50 years old;
ASA grades I to III;
Full term pregnancy and planned cesarean section with transverse incision in the lower segment of the uterus;
Pregnant women who are willing to participate in this study and sign informed consent forms.
Disqualifiers
Have a history of dementia, mental illness, or any central nervous system disorder;
Pregnant women who are addicted to alcohol and drugs;
Difficulty in follow-up or poor patient compliance;
Has taken other investigational drugs or participated in other clinical trials in the three months prior to being selected for the study;
Trial population
Pregnant women planning to undergo cesarean section surgery
Trial design
Design model
Case-only
Time perspective
Prospective
Treatments tested in this trial
Cesarean section
Other interventionObservational study without intervention
Treatment groups
600 Participants
are divided into 1 treatment groupGroup A: Cesarean section surgery1 intervention
Trial outcomes
Primary outcomes
1
Incidence of chronic pain after caesarean section
Assessment of chronic postoperative pain by Brief Pain Inventory from 0 to ten, The higher the score, the stronger the pain
Time frame
2024-01-01-2025-01-01Secondary outcomes
1
Identification of high-risk factors for postoperative inadequate analgesia and PONV in obstetric patients based on machine learning methods
Postoperative pain is represented by NRS score (0-10). The higher the NRS score, the more severe the pain. A NRS score of ≥ 4 is considered insufficient postoperative analgesia. Analyzed the predictive value of 42 variables, including preoperative, intraoperative, and postoperative variables, for postoperative inadequate analgesia.
Time frame
2024-20262
Adverse effects of postoperative analgesia
Incidence and the risk factors of adverse effects of postoperative analgesia, especially postoperative nausea and vomiting
Time frame
2024-20263
Checklist for Chronic pain after cesarean section
Types of chronic pain after cesarean section
Time frame
2024-2026Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov