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临床试验/CTIS2024-510789-17-00
CTIS2024-510789-17-00进行中(未招募)1 期

Perioperative oral analgesia versus intravenous analgesia for knee arthroscopy, a randomized, double-blinded, non-inferiority trial. OVIKA-trial - S68618 - OVIKA-trial S68618

Z Leuven0 个研究点目标入组 108 人开始时间: 2024年3月12日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
108

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
18 至 65+(—)
性别
All

入选标准

  • Minor knee surgery under general anaesthesia, including arthroscopic meniscectomy and synovectomy, diagnostic arthroscopy, meniscus repair and arthroscopic lavage., >=18 years of age, ASA 1-3 suitable for ambulatory surgery, >= 50 kg, Voluntary written informed consent of the participant, Dutch speaking

排除标准

  • History of liver diseases, renal insufficiency, epilepsy, allergy to paracetamol or ibuprofen, Any disorder which, in the Investigator's opinion, might jeopardize the participant's safety or compliance with the protocol, Any prior or concomitant treatment(s) that might jeopardize the participant's safety or that would compromise the integrity of the Trial., Participation in an interventional Trial with an investigational medicinal product (IMP) or device., A contraindication for the use of paracetamol or ibuprofen, Non-compliance of the patient, postive urine pregnancy test in women of childbearing potential

研究者

发起方
Z Leuven

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