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临床试验/NCT03617289
NCT03617289已完成不适用

Efficacy of Magnesium Sulfate on Reducing Renal Colic in the Emergency Department

Henry Ford Health System0 个研究点目标入组 37 人开始时间: 2016年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
37
主要终点
Pain Score Change

研究概览

简要总结

To determine if magnesium sulfate paired with an analgesic medication will improve patient pain from renal colic compared with analgesic alone.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age >18 years old and <100 years old.
  • Patients seen in the Emergency Department at Henry Ford Macomb hospital.
  • Patients that are A+Ox
  • Patients who have typical presentation for renal colic.

排除标准

  • Age <18 years.
  • Patients with a history of dementia, acute delirium or altered mental status.
  • Patients with inability to consent to study or inability to fill questionnaire independently.
  • Patients with chronic kidney disease and allergies to study drugs.
  • Patients that are pregnant (women who are of child-bearing potential will be screened with a urine BHCG).
  • Patients with stroke activation or symptoms.
  • Patients with trauma activations.
  • Patients over the age of 100 years old are excluded as they make up a small percentage of the population and may become identifiable because of their age.
  • Imaging study does not show evidence of ureteral stone.

研究组 & 干预措施

Treatment

Experimental

Receiving Magnesium Sulfate

干预措施: Magnesium Sulfate (Drug)

Placebo

Placebo Comparator

Receiving Dextrose 5% in Water (D5W)

干预措施: D5W (Drug)

结局指标

主要结局

Pain Score Change

时间窗: 1 hour after the completion of treatment medication (Placebo or Study Drug)

We asked the patient's pain score on a scale of 0-10 with 10 being the highest amount of pain and 0 no pain, before and after treatment (approximately 1 hour). Primary Outcome was the change in score before and after treatment.

次要结局

  • Percentage of Participants Requiring Opiates for Additional Pain Control(Any opiate administration required after re-evaluation of pain score after initial treatment with either placebo or study drug)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jason Muir

Principal Investigator

Henry Ford Health System

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