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临床试验/EUCTR2013-005106-64-AT
EUCTR2013-005106-64-AT进行中(未招募)1 期

Continous wound infiltration after hallux valgus surgery - CWI-HVS

Medizinische Universität Innsbruck0 个研究点开始时间: 2014年3月7日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • All patients undergoing a distal metatarsal osteotomy (only Chevron or Scarf) and lateral release of the adductor hallucis muscle with/without concomitant osteotomy of the proximal phalanx of the greater toe (Akin) for idiopathic hallux valgus deformity will be included.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Exclusion criteria are 1. hallux valgus surgery other then mentioned above or concomitant other procedures, 2. denial to participate and give informed consent, 3. patients with neurological diseases that affect the sensory-motor function, 4. patients with any short-term (1 month) previous surgery on affected lower extremity, 5. allergies or other comorbidity that prohibits standardized pain regime (renal insufficiency, severe heart or liver impairment, uncontrolled asthma, history of peptic ulcera ) or 6. patients unwilling to undergo surgery without general anesthesia.

研究者

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