Low Dose Versus High Dose Methylene Blue in Septic Patients

Sponsor
National Cancer Institute, Egypt (Other)
Overall Status
Recruiting
CT.gov ID
NCT06005558
Collaborator
(none)
90
1
3
6.5
13.8

Study Details

Study Description

Brief Summary

The main aim of this study is to examine the various effects of continuous methylene blue infusion in septic cancer patients and to compare it with the traditional infusion of noradrenaline in such patients .

Condition or Disease Intervention/Treatment Phase
  • Drug: Normal saline
  • Drug: Methylene Blue low dose
  • Drug: Methylene Blue high dose
Phase 2/Phase 3

Detailed Description

Exaggerated host response to infection, may result in sepsis, which is life-threatening organ dysfunction . Though considered the number one cause of in-hospital deaths , it can be treatable with early prompt interventions.

The 2021 SSC Guidelines use the Third International Consensus definitions, also known as Sepsis-3. Where sepsis is defined as "life-threatening organ dysfunction caused by a dysregulated host response to infection." Organ dysfunction is evidenced by an increased score of 2 or more in the Quick Sequential [Sepsis-related] Organ Failure Assessment (QSOFA), and septic shock is considered as "a subset of sepsis in which particularly profound circulatory, cellular, and metabolic abnormalities are associated with a greater risk of mortality than with sepsis alone." To diagnose septic shock, an euvolemic patient must require vasopressor support to achieve a mean arterial pressure of at least 65 mm Hg and have a lactate level above 2 mmol/L.

The triad of intravenous fluid, vasopressors and antibiotics in the first hour is the mainstay of septic shock management. Aim of management is to maintain patient hemodynamically stable until antibiotics kick in and fight infection. In case of non-responders, low dose corticosteroids are prescribed. Other drugs need to be studied to also help in cases of non-responders and to improve outcome in general. Methylene blue (MB) is a nitric oxide inhibitor that can counteract the vasodilatation in early septic shock.

Nitric oxide (NO) activates soluble guanylyl cyclase (sGC) which activates cyclic guanosine monophosphate (cGMP)-dependent protein kinases (PKGs) that cause vasodilatation. Methylene blue selectively blocks sGC and inhibits iNOS. Therefore, it selectively acts on the microcirculation.

Onset of action of intravenous MB is 30-60 min. Peak concentration at 30 min. It is excreted through bile and fecal routes plus through the kidneys. Due to the short Plasma half-life of 5-6 hours, some studies used continuous infusion of 0.25-2 mg/kg/h, for up to 3 days following the initial bolus dose

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Treatment
Official Title:
Comparative Study Between High and Low Dose Methylene Blue Infusion in Septic Cancer Patients. A Randomized Blinded Controlled Study
Actual Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Jan 30, 2024
Anticipated Study Completion Date :
Feb 15, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Normal saline

30 patients will receive placebo of 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of Nacl for 72 hours.

Drug: Methylene Blue low dose
A bolus of MB 1mg/kg in 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of 0.25mg/kg/hour for 72 hours.
Other Names:
  • Low dose
  • Drug: Methylene Blue high dose
    A bolus of MB 4mg/kg in 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of 0.25mg/kg/hour for 72 hours.
    Other Names:
  • High dose
  • Active Comparator: methylene blue low dose

    30 patients will receive a bolus of MB 1mg/kg in 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of 0.25mg/kg/hour for 72 hours.

    Drug: Normal saline
    100 ml 0.9% Nacl over 20 minutes, followed by continuous infusion of normal saline for 72 hours.
    Other Names:
  • Control
  • Drug: Methylene Blue high dose
    A bolus of MB 4mg/kg in 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of 0.25mg/kg/hour for 72 hours.
    Other Names:
  • High dose
  • Active Comparator: methylene blue high dose

    30 patients will receive a bolus of MB 4mg/kg in 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of 0.25mg/kg/hour for 72 hours.

    Drug: Normal saline
    100 ml 0.9% Nacl over 20 minutes, followed by continuous infusion of normal saline for 72 hours.
    Other Names:
  • Control
  • Drug: Methylene Blue low dose
    A bolus of MB 1mg/kg in 100ml 0.9% Nacl over 20 minutes followed by continuous infusion of 0.25mg/kg/hour for 72 hours.
    Other Names:
  • Low dose
  • Outcome Measures

    Primary Outcome Measures

    1. Discontinuation of vasopressor [7 days]

      Time for noradrenaline discontinuation

    Secondary Outcome Measures

    1. Mortality [28 days]

      Number of deaths

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients aged ≥ 18 years and ≤ 65 with septic shock as defined by Sepsis-3 criteria (confirmed infection, requiring vasopressor to maintain a mean arterial blood pressure (MAP) ≥ 65 mmHg, and serum lactate > 2 mmol/L after adequate fluid resuscitation), and requiring mechanical ventilation.
    Exclusion Criteria:
    • myocardial infarction or cerebrovascular accident within the last 3 months.

    • severe lung , liver or kidney disease (creatinine >3.5 mg/dL).

    • pregnancy.

    • glucose 6-phosphate-dehydrogenase deficiency.

    • known allergy to MB or food dyes and the use of nitrates within the last 3 days.

    • more than 24 hrs since initiation of norepinephrine.

    • other causes of shock than sepsis .

    • recent intake (4-weeks) of selective serotonin re-uptake inhibitors or MAOi.

    • refusal of the patient guardian to participate.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Cancer Institute Cairo Egypt 12588

    Sponsors and Collaborators

    • National Cancer Institute, Egypt

    Investigators

    • Principal Investigator: Ehab H Shaker, MD, National Cancer Institute (NCI)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ehab Hanafy Shaker, Associate Professor of Anesthesia, ICU and Pain management, National Cancer Institute, Egypt
    ClinicalTrials.gov Identifier:
    NCT06005558
    Other Study ID Numbers:
    • Methylene blue
    First Posted:
    Aug 22, 2023
    Last Update Posted:
    Aug 22, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 22, 2023