Community randomised controlled trial on the effectiveness of two compression bandaging technologies

Queen's University (Canada)0 个研究点目标入组 424 人开始时间: 2006年3月1日最近更新: 2015年1月13日

适应症

试验速览

暂无简介。

•Current information as of 08/05/2009:
•1. 18 years or older, either sex, ability to communicate in English
•2. Could provide written informed consent
•3. Had an ulcer of a minimum duration of 1 week
•4. Had a clinical presentation of venous insufficiency
•5. Had a leg ulcer that measured 0.7 cm in any one dimension
•6. Ankle brachial pressure index greater than or equal to 0.8
•Initial information at time of registration
•1. 18 years or older, either sex, ability to communicate in English
•2. Leg ulcer greater than 1 cm in any one dimension, minimum duration of 1 week, Ankle Brachial Pressure Index (ABPI) greater than 0.7

•Current information as of 08/05/2009:
•1. Had diabetes (taking insulin or an oral hypoglycaemic)
•2. Had failed to improve over a 3-month period after being treated with either bandaging systems prior to the trial
•3. Had been a previous study patient
•4. Were cognitively impaired
•Initial information at time of registration
•1. Diagnosis of diabetes mellitus
•2. Participants who failed to improve over a 3-month period after being treated previously with either of the trial treatments
•3. Previous trial patients
•4. Cognitive impairment

发起方

Queen's University (Canada)