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临床试验/KCT0009540
KCT0009540已完成Unknown

Comparison of the effectiveness of local analgesic injection pump devices and local topical gel-type analgesic agents for postoperative pain control in patients undergoing bariatric metabolic surgery: A randomized controlled trial

Seoul National University Bundang Hospital0 个研究点目标入组 48 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
48

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • The study enrolled participants who satisfied the National Health Insurance criteria for bariatric surgery, which necessitates a body mass index (BMI) of =35 kg/m2 or a BMI of =30 kg/m2 with associated obesity-related complications such as hypertension, hyperlipidemia, diabetes, fatty liver and polycystic ovary syndrome. And individuals aged 19 years or older who voluntarily consented to participate in the study were included.

排除标准

  • The exclusion criteria included: 1) Patients who were currently receiving, or had previously received, any investigational products, or those with medical conditions that could affect the safety and efficacy evaluation of this medical device; 2) Patients with known hypersensitivity to ropivacaine or other amide-type local anesthetics; 3) Patients experiencing severe bleeding or shock; 4) Patients with inflammation at or around the site of injection; 5) Patients suffering from sepsis; 6) Patients requiring intravenous partial anesthesia; 7) Patients who had participated in another clinical study within the past 30 days; 8) Patients considered unsuitable by the investigator for various reasons, such as lack of cooperation; and 9) Patients with contraindications to using ketorolac.

研究者

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