ACTRN12609001080213已完成未知
A randomised controlled trial of Eutectic Mixture of Lidocaine and Prilocaine (EMLA) cream as a primary dressing for the reduction in wound related pain associated with chronic leg ulcers: A pilot study.
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 60
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
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 100 Years（—）
- 性别
- All
入选标准
- •Patient has one or more chronic lower leg ulcer(s) of at least 6 weeks duration and up to 100cm2 in size in total.
- •Patients with low to moderate wound exudate.
- •Numerical Rating Scale pain score = 4 at assessment and/or within the previous week.
- •Patients currently requiring oral analgesics due to previously reported wound-related pain.
- •Patients have the capacity to consent to participation.
- •Patients have the capacity to attend the Community Nursing Procedure clinics.
排除标准
- •Patients scheduled for leg amputation.
- •History of peripheral sensory neuropathy of the feet.
- •Patients that have had or require the use of EMLA cream for debridement of the wound bed within the previous 4 weeks.
- •Patients with suspected wound malignancy or pyoderma gangrenosum, confirmed by biopsy.
- •Patients with diagnosed localized or spreading clinical wound infection.
- •End stage palliative care patients.
- •Allergy to EMLA cream and/or history of local anesthetic drug sensitivity
- •A history of congenital or idiopathic methemoglobinemia
- •Patients on Class III anti-arrhythmic drugs.
- •Severe hepatic disease.
- •Pregnant and/or lactating women.
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