Actively Recruiting
Analysis of the Incidence and Risk Factors of Chronic Pain After Cesarean Section
Led by Huazhong University of Science and Technology · Updated on 2024-11-26
600
Participants Needed
1
Research Sites
152 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Analysis of the Incidence and Risk Factors of Chronic Pain After Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- History of dementia, mental illness, or any central nervous system disorder
- Addiction to alcohol or drugs
- Difficulty in follow-up or poor patient compliance
- Participation in other clinical trials or use of investigational drugs within three months prior to this study
- Serious complications during delivery
- Unable to cooperate with the research for any reason
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tongji hospital
Wuhan, Hubei, China, 430030
Actively Recruiting
Research Team
X
Xianwei Zhang, Doctor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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