Effect of Magnesium Sulphate on Analgesia Following Knee Arthroplasty
赞助:
Ufuk University
合作者:
信息的提供 (责任方):
Baturay Kansu Kazbek,Ufuk University
追踪信息 | |||
---|---|---|---|
首次提交日期 ICMJE | October 2, 2018 | ||
首次发布日期e ICMJE | October 4, 2018 | ||
最后更新发布日期 | October 5, 2018 | ||
预计研究开始日期 ICMJE | November 1, 2018 | ||
预计主要完成日期 | December 1, 2018 (主要结果测量的最终数据收集日期) | ||
目前主要观察指标 ICMJE |
Visual Analogue Score[ Time Frame: T0:(Baseline) Postoperative 1st hour, T1: Change in 2nd, T2: Change in 4th, T3: Change in 6th, T4: Change in 12th, T5: Change in 24th, T6: Change in 36th, T7: Change in 48th, T8: Change in 72nd hours ] measurement of postoperative pain using Visual Analogue Score. Minimum: 0 Maximum: 10. Higher values represent more pain, hence lower values are better |
||
原始主要观察测量 ICMJE | 与当前相同 | ||
目前的二级观察 ICMJE |
|
||
描述性信息 | |||
简略标题 ICMJE | Effect of Magnesium Sulphate on Analgesia Following Knee Arthroplasty | ||
正式标题 ICMJE | The Effect of Magnesium Sulfate Added to Levobupivacaine in Continous Femoral Block on Analgesic Requirements Following Total Knee Arthroplasty | ||
简要概况 | This study is designed to investigate the effect of magnesium sulfate added to levobupivacaine in continuous femoral nerve block following total knee arthroplasty. |
||
详细说明 | Pain after knee arthroplasty is a serious concern. This study was designed to investigate the effect of magnesium sulfate added to levobupivacaine in continuous femoral nerve block on analgesic requirements following total knee arthroplasty. | ||
研究类型 ICMJE | Interventional | ||
研究阶段 | Phase 4 | ||
研究设计 ICMJE | 分配: Randomized 干预模型: Parallel Assignment 干预模型描述: randomized, controlled, prospective 盲法: Interventional 盲法描述: 主要目的: Treatment |
||
适用条件 ICMJE | |||
干预项目 ICMJE |
|
||
研究工具 |
|
||
招募信息 | |||
招募状态 ICMJE | Recruiting | ||
预计入组 ICMJE |
60 | ||
原始预计入组 ICMJE | 与当前相同 | ||
预计研究完成日期 | December 15, 2018 | ||
预计主要完成日期 | December 1, 2018 (主要结果测量的最终数据收集日期) | ||
合格标准 ICMJE | Inclusion Criteria: - scheduled for elective unilateral primary total knee arthroplasty Exclusion Criteria: - Patient refusal to enroll in the study - Patient refusal of neuraxial anesthesia - Existence of contraindications for neuraxial anesthesia - Known history of allergy to any of the study drugs | ||
性别 |
|
||
年龄 | 最小年龄:18 Years ,最大年龄:65 Years | ||
接受健康的志愿者 | 没有 | ||
可入组国家 ICMJE | Turkey | ||
管理信息 | 数据检测委员会 | No | |
研究涉及美国FDA监管的产品 |
研究美国FDA监管的药品: No 研究涉及美国FDA监管的设备产品: No |
||
IPD 共享声明 |
|
||
责任方 | Baturay Kansu Kazbek,Ufuk University | ||
研究赞助商 ICMJE | Ufuk University | ||
合作者 ICMJE | |||
研究员 ICMJE |
|
||
PRS 账户 | Ufuk University | ||
验证日期 | October 2018 | ||
ICMJE 国际医学期刊编辑委员会和 世界卫生组织 ICTRP 要求的元素 |
请使用微信扫码报名