ISRCTN84974248进行中(未招募)2 期
Paracetamol for Acute Renal Injury in Severe Malaria Trial (PARIST)
试验速览
- 阶段
- 2 期
- 状态
- 进行中(未招募)
- 入组人数
- 40
研究概览
简要总结
2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37524553/ (added 01/08/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Children aged >6 months to <12 years
- •2. Positive RDT for P. falciparum malaria at admission
- •3. One of the following features of severe malaria confirmed haemoglobinuria, impaired consciousness and/or severe respiratory distress
- •4. Guardian or parent willing and able to provide consent
排除标准
- •1. Surgery
- •2. Acute trauma or burns
- •3. Known allergy to paracetamol
- •4. Impaired liver function tests
- •5. Known chronic renal failure or suspected non-malarial causes of renal impairment
- •6. Refusal to consent
研究者
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进行中(未招募)
1 期
Paracetamol or NSAID’s in acute disorders of the musculoskeletal tractacute musculoskeletal syndromesMedDRA version: 17.1Level: LLTClassification code 10002182Term: AnalgesiaSystem Organ Class: 100000004865MedDRA version: 17.1Level: LLTClassification code 10033762Term: ParacetamolSystem Organ Class: 100000004848MedDRA version: 17.1Level: HLGTClassification code 10005942Term: Bone and joint injuriesSystem Organ Class: 10022117 - Injury, poisoning and procedural complicationsMedDRA version: 17.1Level: HLTClassification code 10028288Term: Muscle, tendon and ligament injuriesSystem Organ Class: 10022117 - Injury, poisoning and procedural complicationsEUCTR2013-000381-11-NLAcademisch Medisch Centrum
