EUCTR2007-005775-34-GB进行中(未招募)1 期
A Randomised Controlled Trial of Larval Therapy in the Debridement of Leg Ulcers. - Larval Therapy in Leg Ulcer Debridement
ZooBiotic Limited0 个研究点目标入组 172 人开始时间: 2007年11月26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
- 172
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
入选标准
- •People for whom all of the following criteria apply:
- •- Have a sloughy and/or necrotic leg ulcer (slough and/or necrotic tissue estimated to cover a minimum of 25% of the wound) of purely venous or mixed arterial/venous aetiology that can be identified as the reference ulcer; this ulcer must be at least 5cm away from any other ulcer.
- •- Have an ulcer with an area of >/= 2 square cm and < 100 square cm.
- •- Have an ankle brachial pressure index (ABPI) equal to or more than 0.5 where the patient has no concurrent symptoms precluding compression.
- •- Are aged 18 years or above.
- •- Are willing and able to give informed written consent.
- •- People with well controlled diabetes mellitus are eligible (HbA1c equal to or less than 10% measured within the previous 12 weeks). The wound should be on or above the malleoli to ensure it is not a diabetic foot wound.
- •- People with rheumatoid arthritis are eligible to particpate provided they have ulcers that are deemed to be venous in origin.
- •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 86
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 86
排除标准
- •People who:
- •- Have previously been entered into the intervention phase of the trial.
- •- Are women of child bearing potential.
- •- Are pregnant or lactating women.
- •- Are allergic to hydrogel dressings or any of their components.
- •- Have grossly oedematous legs, which in the opinion of the recruiting health care professional would not be suitable for treatment with larval therapy and/or hydrogel.
- •- Patients on anti-coagulant therapy i.e. Warfarin and Heparin (note that patients on prophylactic low molecular weight Heparin may be included).
- •- People with diabetes mellitus whose blood sugar is not well controlled (HbA1c greater than 10% as measured within the past 12 weeks).
- •- Patients with clinical signs of infection on the day of enrolment.
- •- Patients on antibiotics.
- •- Patients who have deep wounds with exposed bone, tendon or muscle.
- •- People for whom particpation would not be in their best interests, in the opinion of the recruiting health professional.
研究者
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