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临床试验/NCT07048782
NCT07048782尚未招募不适用

Development and Validation of a Risk Prediction Model for Postoperative Visceral Pain in Abdominal Surgery Patients

The Second Affiliated Hospital of Chongqing Medical University1 个研究点 分布在 1 个国家目标入组 1,135 人开始时间: 2025年7月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,135
试验地点
1
主要终点
Pain intensity after surgery

研究概览

简要总结

This study aims to investigate the factors influencing the risk of postoperative visceral pain in patients undergoing abdominal surgery. The goal is to develop and validate a predictive model for assessing the risk of postoperative visceral pain, in order to guide individualized preoperative interventions and pain management strategies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing elective abdominal surgery under general anesthesia (including gynecological procedures and general surgery such as gastrointestinal, hepatobiliary, etc.);
  • Aged between 18 and 70 years;
  • Classified as American Society of Anesthesiologists (ASA) physical status II-III;
  • Expected surgery duration ≥ 2 hours.

排除标准

  • History of previous abdominal surgery;
  • Diagnosed with chronic pain;
  • Long-term use of analgesics or other psychotropic medications;
  • Preoperative emergency condition;
  • Presence of severe comorbidities involving major organ systems;
  • Failure to complete postoperative pain follow-up.

结局指标

主要结局

Pain intensity after surgery

时间窗: From end of surgery to 48 hours postoperatively

Pain intensity will be recorded at 6, 12, 24, and 48 hours after surgery. At each time point, the Numerical Rating Scale (NRS) pain score will be assessed both at rest and during coughing. Pain intensity was assessed using number rating scale (0-10, higher score represents worse pain intensity)

次要结局

  • Postoperative Length of Hospital Stay(From end of surgery to hospital discharge (up to 30 days))
  • Postoperative Analgesic Use(From end of surgery to hospital discharge (up to 30 days))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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