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临床试验/NCT07716956
NCT07716956尚未招募不适用

Effect of Targeting Upper Normal Serum Magnesium Levels on Norepinephrine Requirements in Septic Shock Patients: a Randomized Controlled Trial.

Alexandria University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Total cumulative dose of norepinephrine

研究概览

简要总结

The goal of this clinical trial is to assess the effect of targeting upper normal serum magnesium levels on norepinephrine requirements in adult patients with septic shock.

The main questions it aims to answer are:

  1. Does maintaining upper normal serum magnesium levels lower the total cumulative dose and duration of norepinephrine therapy?
  2. Does this approach reduce the intensive care unit (ICU) length of stay, duration of mechanical ventilation and mortality?

This study will compare an intervention group to a control group to see the effect of targeting upper normal serum magnesium levels.

Participants will:

  • Have their serum magnesium levels assessed at baseline (Day 0), at three-day intervals (Days 3, 6, 9) thereafter and on the day of norepinephrine discontinuation.
  • Receive individualized intravenous magnesium sulfate infusions to achieve and maintain the target serum magnesium levels.
  • Have their demographic data collected and be monitored closely for clinical data, vital signs, Mean Arterial Pressure (MAP), urine output and laboratory parameters.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • Male and female adult patients (aged ≥18 years) diagnosed with septic shock.
  • Resistant septic shock that requires corticosteroids.

排除标准

  • Pregnancy.
  • Baseline hypermagnesemia (serum magnesium level > 2.3 mg/dL).
  • Renal impairment with creatinine clearance (CrCl) < 10 ml/min.
  • Mixed shock.

研究组 & 干预措施

Control group

Active Comparator

Patients will receive standard care to maintain serum magnesium levels (1.7 - 1.9 mg/dL).

干预措施: standard care treatment (Other)

Intervention group

Experimental

Patients will receive intravenous magnesium sulfate infusion to achieve and maintain upper normal serum magnesium levels (2.0 - 2.3 mg/dL).

干预措施: magnesium sulfate (Drug)

结局指标

主要结局

Total cumulative dose of norepinephrine

时间窗: Up to 60 days.

Total cumulative dose of norepinephrine administered to the patient, measured in µg/kg.

Duration of norepinephrine therapy

时间窗: Up to 60 days.

The time from the initiation of norepinephrine until discontinuation, measured in hours.

次要结局

  • ICU length of stay(Up to 60 days.)
  • Duration of mechanical ventilation(Up to 60 days.)
  • Mortality(Up to 60 days.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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