Actively Recruiting

Age: 20Years - 50Years
FEMALE
ID06704490

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

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Persistent postoperative pain is a significant issue worldwide, particularly following cesarean section surgery. This observational study aims to understand how often and in what ways chronic pain occurs after cesarean section at 3, 6, and 12 months post-surgery. It also explores how factors around the time of surgery relate to chronic pain and examines the connection between long-lasting pain and postpartum depression in mothers. The study observes women who have undergone cesarean section with a specific surgical approach (transverse incision in the lower uterus). Participants will be followed prospectively without any intervention, focusing on data collection related to their pain experience and other postoperative conditions. This research will use data modeling and regression analysis to identify risk factors for chronic pain and associated complications. Participants will be monitored through follow-up visits up to 12 months after surgery, during which their pain levels and any signs of depression will be assessed. Researchers will collect information on pain incidence and characteristics, adverse effects related to pain management, and other relevant outcomes. The total participation period spans from surgery through one year of postoperative observation, allowing detailed tracking of symptoms and their impact on quality of life.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 20Years - 50Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • History of dementia, mental illness, or any central nervous system disorder
  • Pregnant women addicted to alcohol and drugs
  • Difficulty in follow-up or poor patient compliance
  • Participation in other clinical trials or use of investigational drugs within the past three months
  • 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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery

Duration - Day of surgery

Participants who undergo cesarean section surgery are observed without intervention as part of the study.

1 visit (in-person)

Post-operative Follow-up

Duration - Up to 2 years

Participants are followed after surgery to monitor for the incidence and risk factors of chronic pain and other postoperative outcomes.

Periodic visits depending on clinical follow-up

Trial Site Locations

Total: 1 location

1

Tongji hospital

Wuhan, Hubei, China, 430030

Actively Recruiting

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Research Team

X

Xianwei Zhang, Doctor

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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Published Research Related To This Trial

Method of delivery and pregnancy outcomes in Asia: the WHO global survey on maternal and perinatal health 2007-08.

Pisake Lumbiganon, Malinee Laopaiboon, A Metin Gülmezoglu...

https://pubmed.ncbi.nlm.nih.gov/20071021