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Efficacy and Safety of Methylene Blue in the Treatment of Severe Septic Shock

RecruitingNAAges any - anyAllFirst Affiliated Hospital of Zhejiang University
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In plain words

What the trial is, and whether it could suit you

The goal of this clinical trial is to investigate whether methylene blue injection can safely and effectively improve the survival rate of patients with severe septic shock, shorten the duration of norepinephrine use, reduce the dosage of vasopressors, promptly correct hemodynamics, and improve tissue perfusion and organ function impairment.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. Age โ‰ฅ 18 years. 2. Meets the Sepsis 3.0 criteria for septic shock: patients with infection who, despite adequate fluid resuscitation, require vasopressor therapy to maintain a mean arterial pressure (MAP) of โ‰ฅ 65 mmHg and have a blood lactate concentration \> 2 mmol/L. 3. Diagnosed with septic shock and started on norepinephrine within 24 hours. 4. Requires a norepinephrine dose of โ‰ฅ 0.1 ฮผg/kg/min to maintain a MAP of โ‰ฅ 65 mmHg. Exclusion Criteria: 1. Pregnant or breastfeeding women. 2. Individuals allergic to methylene blue or any components of the methylene blue injection. 3. Individuals with a personal or family history of glucose-6-phosphate dehydrogenase (G6PD) deficiency. 4. Patients with an expected survival time of less than 48 hours. 5. Patients who have been on norepinephrine for more than 24 hours.
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What it tests

  • Methylene Blue Intervention Group
  • Normal Saline Control Group
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Where

1 site
The First Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, China
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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