跳至主要内容
临床试验/CTRI/2026/01/100301
CTRI/2026/01/100301尚未招募2 期

A randomized clinical study of the effects of early use of Methylene Blue on Noradrenaline dose in shock.

Subharti Medical College1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年1月26日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
CHANGE IN NORAD DOSE AFTER STARTING VASOPRESSIN AND METHYLENE BLUE

研究概览

简要总结

THIS STUDY IS A RANDOMIZED CLINICAL STUDY OF THE EFFECTS OF EARLY USE OF METHYLENE BLUE ON NORADRENALINE DOSE IN  SHOCK WHERE THERE WILL BE A COMPARISON BETWEEN TWO GROUPS WHERE ONE WILL RECEIVE ONLY VASO AND ANOTHER VASO+ METHYLENE BLUE AFTER A CERTAIN DOSE OF NORAD.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patient admitted in ICU with shock and requires noradrenaline to maintain a mean arterial pressure (MAP) of greater than or equal to 65 mm Hg after appropriate fluid resuscitation.

排除标准

  • relatives/patient refused to provide consent With unstable coronary artery syndrome, stroke chronic renal failure requiring dialysis, malignancy or irreversible illness with a high mortality risk, acute mesenteric ischemia, pregnancy known hypersensitivity to norepinephrine or Methylene Blue or Vasopressin Glucose-6-phosphate dehydrogenase (G6PD) deficiency.

结局指标

主要结局

CHANGE IN NORAD DOSE AFTER STARTING VASOPRESSIN AND METHYLENE BLUE

时间窗: 0 hours, 6 hours, 12 hours, 24 hours

次要结局

  • Changes in Lactate Levels,(Urine Output)

研究者

发起方
Subharti Medical College
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Akshita

Subharti medical college

研究点 (1)

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