ACTRN12623000936628招募中4 期
Efficacy of self-administered inhaled methoxyflurane (Penthrox®) as pre-injection analgesia in Podiatry Outpatients: A blinded, randomised study.
Claire Huxtable0 个研究点目标入组 40 人开始时间: 2023年8月30日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 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
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •o18 years of age and over
- •oA painful ingrown toenail which requires a minor surgical procedure
- •oAbility to self-administer methoxyflurane via a hand-held Penthrox® inhaler.
排除标准
- •oA documented history of cognitive impairment or are otherwise unable to give informed consent
- •oAllergy to methoxyflurane or any other medication or agent required for the procedure
- •oA personal or familial history of malignant hyperthermia
- •oPrevious history of a significant head injury
- •oSignificant renal impairment (eGFR<60mL/min)
- •oSignificant cardiac or respiratory illnesses
- •oWomen who are pregnant, planning to become pregnant or breastfeeding
- •oPatients taking concurrent drugs with known clinically significant nephrotoxic effects (patients taking tetracyclines, aminoglycosides, colistin, amphotericin B, barbiturates, alcohol, isoniazid and rifampicin will be excluded).
- •oPatients who have received methoxyflurane on the day prior to the procedure or 15 mL (5 bottles) in the week prior to the procedure.
- •oNeurological Assessment: Absent protective sensation upon monofilament testing.
- •oVascular Assessment: Clinically significant Peripheral Arterial Disease.
- •oPatients who are not willing or able to fast for 6 hours prior to the planned procedure.
研究者
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