CTRI/2019/09/021152已完成3 期
Randomized Controlled Trial to compare two different doses of Folinic acid (leucovorin) in Methotrexate Toxicity - FLIMT
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 38
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
入选标准
- •1 A patient prescribed weekly or the biweekly dose of tablet or parenteral Methotrexate (up to 50 mg per week) for rheumatic or dermatologic or gastrointestinal disease
- •2 Patient having methotrexate hematologic Toxicity defined as EITHER WBC less than 2000 AND OR Platelet count less than 50000 per microlitre (with or without mucositis)
- •3 Either inadvertent overdose OR renal dysfunction
排除标准
- •1 Patient not consenting for the study
- •2 Patient being treated with High Dose Methotrexate regimen.
- •3 Patient <12 years of age
- •4 Patient already received more than one dose of folinic acid
研究者
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