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临床试验/CTIS2024-511818-21-00
CTIS2024-511818-21-00进行中(未招募)1 期

Anesthetic block of the erector muscles of the lumbar spine to relieve acute lumbar pain: pilot study - BLOCLOMB

Sante Atlantique0 个研究点目标入组 40 人开始时间: 2024年5月2日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
40

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

  • Male or female, Age = 18 years, Patient with lumbago lasting less than 7 days despite analgesic / NSAID treatment., Patient with NS pain > 6, Patient with Oswestry score = 30, Patient informed of the trial and having signed the informed consent form prior to any trial-specific procedure, Patient willing and able to undergo all planned examinations and procedures in compliance with the clinical trial protocol, Patient affiliated to a social security or any health insurance

排除标准

  • Presence of red flag (non-disc lumbago): o Motor deficit or signs of horsetail irritation o Inflammatory pain waking up in the 2nd half of the night o Tumoral context o Infectious context or fever o Altered general condition o Traumatic context o Osteoporotic context, Pregnant or breastfeeding woman or woman refusing effective contraception, Patient deprived of liberty or under legal protection (guardianship or curatorship), Patient participating in another clinical research protocol involving a drug or medical device, Patient unable to follow the protocol, as judged by the investigator, Patient refusing to participate in the study, Risk of infection, Patient with poor local skin condition, Patient on AVK or anti-Xa anticoagulation, or bleeding disorder (antiaggregants authorized), Patients with hypersensitivity to Ropivacaine or any of its excipients: Sodium chloride, hydrochloric acid sodium hydroxide, Patient with sciatica, Patient with chronic respiratory insufficiency, Patient with cardiac rhythm disorders, Pregnant or breastfeeding woman or woman refusing effective contraception

研究者

发起方
Sante Atlantique

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