RecruitingNCT06704490

Analysis of the Incidence and Risk Factors of Chronic Pain After Cesarean Section


Sponsor

Huazhong University of Science and Technology

Enrollment

600 participants

Start Date

Feb 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

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

Sex: FEMALEMin Age: 20 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating how often women develop chronic pain at the site of their cesarean section scar after a planned C-section, and what risk factors are associated with it. **You may be eligible if...** - You are between 20 and 50 years old - You are having a planned cesarean section with a low horizontal incision - Your pregnancy is at full term - You are willing to participate and sign the consent form - Your overall health status is ASA grade I to III (ranging from healthy to having some systemic health conditions) **You may NOT be eligible if...** - You have a history of dementia, mental illness, or a brain or nervous system disorder - You are addicted to alcohol or drugs - You have participated in another clinical trial in the past 3 months - You experience serious complications during delivery - You are unlikely to be able to complete follow-up visits Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERCesarean section

Observational study without intervention


Locations(1)

Tongji hospital

Wuhan, Hubei, China

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NCT06704490


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