ACTRN12620000652976撤回未知
Protocol for an effectiveness-implementation hybrid trial to assess the effectiveness of implementing applied muscle tension during plasma apheresis on reducing the incidence of syncope and presyncope symptoms: a cluster randomised step-wedged study
适应症
试验速览
- 阶段
- 未知
- 状态
- 撤回
- 入组人数
- 13,000
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 o limit（—）
- 性别
- All
入选标准
- •1. Donor centres with minimum attendance of 54 plasma donors per week
- •2. Donor centres using the Aurora machine used as standard plasmapheresis practice for a minimum of 4 weeks to 3 months depending on guidance from the Clinical Hypervigilance team and the Donor Services Leadership Team
- •PARTCIPANTS
- •1. Eligible for plasma donation as per the current ‘Guidelines for the Selection of Blood Donors’ (GSBD)
- •2. Plasmapheresis donation
- •3. Consent to participate in study (survey component only)
排除标准
- •1. Plasma only donor centres
- •2. Donor mobile units (DMUs) and demountable mobile units
- •3. Participation in another research study (R&D or Marketing) that may interfere with donor recruitment and the outcomes under investigation
- •4. Donor Services Leadership Team consider the donor centre not appropriate for participation (e.g. centre undergoing renovations, relocation)
- •PARTICIPANTS
- •1. Donors not donating plasma by apheresis (e.g., whole blood, platelets, sample only)
- •2. Australian Red Cross Lifeblood staff members
研究者
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