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临床试验/EUCTR2007-005775-34-GB
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

发起方
ZooBiotic Limited

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