EUCTR2012-005573-31-BE进行中（未招募）不适用
Effects of the combination of dexamethasone or clonidine with ropivacaine during a popliteal block : a prospective double blind randomized trial. - POP 1 study
zna middelheim0 个研究点开始时间: 2013年1月7日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •Inclusion criteria are:
- •* physical status ASA I-II (Table 1), age 16-70 years
- •* patient scheduled for elective fore foot surgery (hallux valgus)
- •* scheduled surgery time between 20 and 90 min
- •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 100
- •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:
- •ASA III-IV-V
- •Chronic renal insufficiency (serum creatinine > 0.45 mg/dl);
- •Surgery duration of less than 20 minutes and longer than 90 minutes ;
- •Known coagulation disorders;
- •Known allergy to local anethetics;
- •Preoperative use of analgetics/opioids;
- •(Chronic) pain syndromes;
- •Psychiatric patients;
- •Peripheral neuropathy;
- •Diabetes Mellitus;
- •Gastric or duodenal ulcers;
- •Contraindications to loco-regional anesthesia (local or systemic sepsis, operator inexperience and patient or parent refusal)
- •Plasma haemoglobin concentration below 8 g/dl
研究者
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