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CTRI Number  CTRI/2025/02/080239 [Registered on: 10/02/2025] Trial Registered Prospectively
Last Modified On: 04/02/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Diagnostic
Other (Specify) [Proof of concept study]  
Study Design  Single Arm Study 
Public Title of Study   A test done to check the blood flow to the gut organs in the patients with severe blood infection using a liver dye  
Scientific Title of Study   Indo cyanine green retention test to study the effect of methylene blue on splanchnic circulation in patients with refractory septic shock proof of concept study.  
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
4589_Protocol Version 1.1_dated 30.10.2024  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Atul Kulkarni 
Designation  Professor and Head, Division of Critical Care Medicine 
Affiliation  Tata Memorial Centre 
Address  Department of Anaesthesia, Critical Care and Pain, Second Floor, Main Building, Dr. E Borges Road, Tata Memorial Hospital, Parel, Mumbai

Mumbai
MAHARASHTRA
400012
India 
Phone  9869077526  
Fax    
Email  kaivalyaak@yahoo.co.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr Atul Kulkarni 
Designation  Professor and Head, Division of Critical Care Medicine 
Affiliation  Tata Memorial Centre 
Address  Department of Anaesthesia, Critical Care and Pain, Second Floor, Main Building, Dr. E Borges Road, Tata Memorial Hospital, Parel, Mumbai

Mumbai
MAHARASHTRA
400012
India 
Phone  9869077526  
Fax    
Email  kaivalyaak@yahoo.co.in  
 
Details of Contact Person
Public Query
 
Name  Dr A Koushik 
Designation  DM Critical care resident 
Affiliation  Tata Memorial Centre 
Address  Department of Anaesthesia, Critical Care and Pain, Second Floor, Main Building, Dr. E Borges Road, Tata Memorial Hospital, Parel, Mumbai

Mumbai
MAHARASHTRA
400012
India 
Phone  8008204879  
Fax    
Email  arvakoushik@gmail.com  
 
Source of Monetary or Material Support  
Dept of Anaesthesia, Critical care and Pain, OT complex, Second floor, Main Building, Tata Memorial Hospital, Parel, Mumbai 400012 India 
 
Primary Sponsor  
Name  TMC Research Administrative Council 
Address  Tata Memorial Centre, Parel, Mumbai 400012, Maharashtra, India  
Type of Sponsor  Research institution and hospital 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Atul Kulkarni  Tata Memorial Hospital   Department of Anesthesia Critical care and Pain, Major OT complex, Second floor, Main Building, Tata Memorial Centre Dr E Borges Road, Parel,Mumbai-400012
Mumbai
MAHARASHTRA 
9869077526

kaivalyaak@yahoo.co.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee II   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: A419||Sepsis, unspecified organism, (2) ICD-10 Condition: R57||Shock, not elsewhere classified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Indocyanine green test  ICG is reconstituted with the provided diluent to form solution of concentration 1 ml containing 5 mg of ICG . The dose given to the patient is calculated based on body weight 0.5 mg/kg. Total dye is injected through a peripheral vein access and blood sample is collected in plain vial every 5 minutes after dye injection for 20 min. The blood samples are sent for laboratory for the results. The test will be done twice in each patient, prior to methylene blue administration and 1 hour after methylene blue administration and compare these two test results with the normal values. 
Comparator Agent  Nil  This is single arm study. So there is no comparator 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  90.00 Year(s)
Gender  Both 
Details  Inclusion criteria:
1.Adults admitted to the ICU with refractory septic shock who are receiving methylene blue therapy
2.Consent from the LAR to participate in the study  
 
ExclusionCriteria 
Details  Exclusion criteria:
1.Known allergy to methylene blue or indocyanine green
2.Known G6PD deficiency or any hemolytic disorder
3.Pre existing cardiovascular disease
4.Previously recorded ejection fraction less than 40 percentage
5.Patients with survival expectancy less than 24 hours
6.Patients whose LAR refuse consent 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Effect of methylene blue on splanchnic circulation in patients with refractory shock  1. Within 30 min of starting the methylene blue
2. 1 hour after starting the methylene blue 
 
Secondary Outcome  
Outcome  TimePoints 
ICU and hospital mortality, SOFA score, GI bleed incidence, Need for renal replacement therapy and RRT free days  At discharge from ICU and hospital 
 
Target Sample Size   Total Sample Size="10"
Sample Size from India="10" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   17/02/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Vasopressors are vital in the treatment of fluid-unresponsive septic shock. Current evidence suggests the use of noradrenaline as the first line vasopressor, followed by other drugs such as vasopressin, adrenaline, angiotensin-II, and terlipressin. There is an interest in the use of methylene blue infusion as a vasoconstrictor. One of the theoretical adverse effects of vasopressor therapy is their vasoconstrictive effect on the splanchnic circulation. This may impair already compromised gut circulation, leading to translocation of bacteria across the ischemic gut endothelium, worsening the septic shock. It was believed previously that noradrenaline worsens the gut and renal perfusion due to splanchnic vasoconstriction.However, noradrenaline actually increases the renal and gut perfusion by increasing the cardiac output as well as mean arterial pressure. 

            The inflammatory mediators such as endotoxins, cytokines,tumor necrosis factor alpha and interleukin-2 can induce a calcium-independent induced nitric oxide synthase (iNOS), leading to a sustained production of nitric oxide that does not respond tonegativefeedback mechanisms.  Nitric oxide causes significant vasodilatation leading to hypotension in patients with septic shock. Increased levels of NO are associated with diminished response to vasopressor therapy leading to need for high dose of vasopressors, altered regional blood flow distribution, increased capillary leakage and multiple organ dysfunction.

            Methylene blue (MB) is an inhibitor of the inducible nitric oxide synthase (iNOS) and its downstream enzyme soluble guanylate cyclase (sGC), leading to vasoconstriction. Through its indirect pressor effects, it has been shown to restore vasoregulation in conditions of NO upregulation and inturn reduces the vasopressors dose.

Indocyanine green (ICG) is a fluorescent dye with high protein binding capacity which is exclusively metabolized in the liver and excreted in the bile. ICG retention test is often used to determinesplanchnic perfusion. Splanchnic blood flow can be estimated from the extraction of ICG from the plasma by the liver, this indirectly gives an idea about splanchnic circulation. In our hospital, ICG retention test is routinely used to assess the function of liver in patients planned for hepatic resection using peripheral blood sampling (without canulation of the hepatic vein) and has been standardized for this purpose. We intend to use this test for assessing the effect of MB on the splanchnic circulation.

            From some recent studies, methylene blue (MB) seems to be effective as an adjunct for patients on dual vasopressor therapy (refractory septic shock). We are currently evaluating use of MB as an adjunct to Noradrenaline and Vasopressin in such patients in our ICU. (IEC Project no. 4216). Since we are using MB in these patients, we aim to evaluate the splanchnic perfusion in patients receiving methylene blue using ICG retention. This is a proof of concept study and we will recruit 10 patients, who are randomised in our other study to receive MB.

 
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