Interventions to reduce unnecessary caesarean sections in healthy women and babies.
Ana Pilar Betrán, Marleen Temmerman, Carol Kingdon...
https://pubmed.ncbi.nlm.nih.gov/30322586Actively Recruiting
Led by Huazhong University of Science and Technology · Updated on 2024-11-26
600
Participants Needed
1
Research Sites
N/A
Total Duration
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
Analysis of the Incidence and Risk Factors of Chronic Pain After Cesarean Section
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants who undergo cesarean section surgery are observed without intervention as part of the study.
1 visit (in-person)
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
Total: 1 location
1
Tongji hospital
Wuhan, Hubei, China, 430030
Actively Recruiting
X
Xianwei Zhang, Doctor
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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