| 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
|
|
|
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
|
|
|
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. |