DRKS00022186招募中2 期
Safety and Performance Evaluation of Seraph 100 Microbind Affinity Blood Filter (Seraph 100) in the reduction of pathogen load from the blood in septic patients with suspected, life-threatening bloodstream infection - CP015
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 232
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
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 90 Years(—)
- 性别
- All
入选标准
- •1. Patients with sepsis and suspected bloodstream infection
- •2. Be = 18 years old and =90 years old
- •3. Adults receiving IV antibiotic therapy
- •4. Increase of at least two points of the Sequential Organ Failure Assessment (SOFA) score
- •5. Subjects that presents Procalcitonin (PCT) levels >0,5 ng/m
排除标准
- •1. Subject is currently participating in another clinical investigation
- •2. Pregnant or nursing subjects and those who plan pregnancy during the clinical investigation follow-up period
- •3. Presence of comorbid conditions, or other medical, social, or psychological conditions that, in the investigator’s opinion, could limit the subject’s ability to participate in the clinical investigation or to comply with follow-up requirements, or impact the scientific soundness of the clinical investigation results
- •4. Antibiotic IV treatment > 12 h before screening
- •5. Have neutropenia (absolute neutrophil count <500 cells/uL
- •6. Have Child-Pugh Class C cirrhosis
- •7. Have platelet count <30.000/uL
- •8. Contraindications for heparin sodium for injection
- •9. Subjects demonstrating any contraindication for this treatment as described in the IF
研究者
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