NCT07558512已完成不适用
Risk Factors and a Predictive Nomogram for Acute Moderate-to-severe Postoperative Pain Afte Achilles Tendon Surgery: A Retrospective Cohort Study
Min Li1 个研究点 分布在 1 个国家目标入组 489 人开始时间: 2026年4月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 489
- 试验地点
- 1
研究概览
简要总结
This is a single-center retrospective cohort study to identify independent risk factors and develop a predictive nomogram for moderate-to-severe pain within 24 hours after Achilles tendon surgery.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 18 years; American Society of Anesthesiologists (ASA) physical status classification Ⅰ~Ⅲ;
- •Clinically diagnosed with Achilles tendon rupture, Achilles tendinopathy, insertional Achilles tendinitis, Haglund's deformity, or other Achilles tendon disorders;
- •Undergoing open or arthroscopic Achilles tendon surgery;
- •Conscious and able to cooperate in surgery and postoperative pain assessment;
- •Complete and accessible case data related to surgery, anesthesia, and postoperative pain assessment;
- •Completion of at least 24 hours of standardized pain monitoring and clinical follow-up after surgery
排除标准
- •Missing or incomplete key clinical data such as pain assessment, surgery and anesthesia;
- •Failure to complete 24-hour standardized pain monitoring after surgery; Perioperative unplanned secondary surgery or transfer to the intensive care unit (ICU);
- •Patients with mental illness, cognitive dysfunction, or language communication barrier; History of alcohol or drug addiction Pain due to other acute or chronic diseases;
- •Bilateral Achilles tendon surgery Concurrent surgery for other lower extremity injuries
研究者
Min Li
Chief Physician, Department of Anesthesiology
Peking University Third Hospital
研究点 (1)
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