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

Last updated: November 24, 2024
Sponsor: Huazhong University of Science and Technology
Overall Status: Active - Recruiting

Phase

N/A

Condition

Pain

Post-surgical Pain

Acute Pain

Treatment

Cesarean section

Clinical Study ID

NCT06704490
chronic postoperative pain
  • Ages 20-50
  • Female

Study 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 Criteria

Inclusion

Inclusion Criteria:

  • Age range from 20 to 50 years old;

  • ASA grades I to III;

  • Full term pregnancy and planned cesarean section with transverse incision in thelower segment of the uterus;

  • Pregnant women who are willing to participate in this study and sign informedconsent forms.

Exclusion

Exclusion Criteria:

  • 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 inthe three months prior to being selected for the study;

  • Serious complications occur during delivery;

  • Unable to cooperate with the research for any reason.

Study Design

Total Participants: 600
Treatment Group(s): 1
Primary Treatment: Cesarean section
Phase:
Study Start date:
February 01, 2024
Estimated Completion Date:
December 31, 2026

Connect with a study center

  • Tongji hospital

    Wuhan, Hubei 430030
    China

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.