JPRN-jRCTs032220597招募中Unknown
Efficacy and safety of poly acrylic acid-poly vinylpyrrolidone complexes for bleeding time after arterial venous fistula decannulation in hemodialysis patients - PAA-PVP trial
Yamamoto Suguru0 个研究点目标入组 50 人开始时间: 2023年1月31日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 18age old 至 ot applicable(—)
- 性别
- All
入选标准
- •Patients who meet all the inclusion criteria as below,
- •1. Patients who can obtain written informed consent to participate in this study based on their free will.
- •2. Patients who are more than 18 years old.
- •3. Patients undergoing regular hemodialysis treatment 3 times a week and for 3-5 hours each session using internal shunt.
- •4. Patients who use heparin as anti-coagulant for hemodialysis treatment
- •5. Patients whose bleeding time after decannulation at the end of hemodialysis treatment is 10 minutes using regular hemostasis pad and band.
排除标准
- •Patients who meet any exclusion criteria as below.
- •1. Patients who participate in other clinical studies.
- •2. Patients who are pregnant or want pregnancy.
- •3. Patients who do not use internal shunt as vascular access.
- •4. Patients who use fingers or use band for more than 10 minutes for hemostasis after decannulation at the end of hemodialysis treatment.
- •5. Patients who have serious skin disease.
- •6. Patients who have the plan to start anti-coagulant/anti-platelet therapy
- •7. Patients that the investigators decide inappropriate to join the study.
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