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CTRI Number  CTRI/2024/09/074087 [Registered on: 20/09/2024] Trial Registered Prospectively
Last Modified On: 19/09/2024
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia 
Study Design  Other 
Public Title of Study   Enhancing Patient Outcomes in Complex Surgeries: A Comparative Analysis of Goal-Directed Fluid Therapy versus Standard Protocols in Cytoreductive Surgery with Hyperthermic Intraperitoneal Chemotherapy 
Scientific Title of Study   Assessing the Impact of Goal-Directed Fluid Therapy Protocol on Perioperative Outcomes in Patients Undergoing Cytoreductive Surgery with Hyperthermic Intraperitoneal Chemotherapy: A Comparison with Standard Institutional Fluid Therapy Protocol 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Raghav Gupta 
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences (AIIMS)  
Address  Room No 126, Academic Block, National Cancer Institute (NCI), AIIMS, Jhajjar, Haryana

Jhajjar
HARYANA
124105
India 
Phone  8130622963  
Fax    
Email  raghavgupta88@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Raghav Gupta 
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences (AIIMS)  
Address  Room No 126, Academic Block, National Cancer Institute (NCI), AIIMS, Jhajjar, Haryana


HARYANA
124105
India 
Phone  8130622963  
Fax    
Email  raghavgupta88@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Raghav Gupta 
Designation  Assistant Professor 
Affiliation  All India Institute of Medical Sciences (AIIMS)  
Address  Room No 126, Academic Block, National Cancer Institute (NCI), AIIMS, Jhajjar, Haryana


HARYANA
124105
India 
Phone  8130622963  
Fax    
Email  raghavgupta88@gmail.com  
 
Source of Monetary or Material Support  
Intramural AIIMS, New Delhi 
 
Primary Sponsor  
Name  AIIMS, New Delhi 
Address  All India Institute of Medical Sciences (AIIMS), Ansari Nagar, New Delhi-110029 
Type of Sponsor  Research institution 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 2  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Raghav Gupta  Department of Onco-Anesthesia and Palliative Medicine  Department of Onco-Anesthesia and Palliative Medicine, DR BRAIRCH, AIIMS, New Delhi
New Delhi
DELHI 
8130622963

raghavgupta88@gmail.com 
Dr Raghav Gupta  National Cancer Institute (NCI), AIIMS, Jhajjar, Haryana  National Cancer Institute (NCI), AIIMS, Badsa, Jhanjrola, Haryana 124105
Jhajjar
HARYANA 
8130622963

raghavgupta88@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institute Ethics Committee AIIMS  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: C169||Malignant neoplasm of stomach, unspecified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Gold Directed Fluid Therapy   Gold Directed Fluid Therapy using flotrac/vigileo. THis monitoring will be done throughout the surgery and in the post-operative period in ICU.  
Comparator Agent  Standard fluid therapy   Standard fluid therapy using institutional protocol  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  70.00 Year(s)
Gender  Both 
Details  1. Agree to participate in the study and sign written informed consent.
2. ASA-PS grade I /II or III patients posted for CRS and HIPEC surgery.
 
 
ExclusionCriteria 
Details  1.Known case of liver dysfunction or renal dysfunction
2.Known coagulation disorder
3.COPD with FEV1
4.Left Ventricular Ejection Fraction
5.Allergic to any drug used during the study 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
Post-operative Renal complications in terms of AKIN classification and improvement in AKI  At baseline and immediately after surgery and 24 hrs post-surgery.  
 
Secondary Outcome  
Outcome  TimePoints 
a) Intraoperative and post-operative serum lactate levels.
b) Post-operative length of stay in the Intensive Care Unit (ICU) until the patient is deemed fit for discharge.
c) 30-day mortality rate after the surgery. 
a) 24 hours
c) 30 days  
 
Target Sample Size   Total Sample Size="60"
Sample Size from India="60" 
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)   30/09/2024 
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  

Peritoneal carcinomatosis (PC) represents a widespread metastatic dissemination throughout the abdomen and pelvis of many organ-based malignancies, particularly carcinomas of the gastrointestinal tract and ovaries. The most common malignancies that can develop peritoneal carcinomatosis include (1) mucinous appendiceal neoplasms and appendix cancer, (2) colorectal cancer, (3) ovarian cancer and primary peritoneal carcinomas, (4) peritoneal mesothelioma, (5) gastric cancer, (6) small bowel cancer, (7) pancreatic cancer, and (8) sarcomas.

In the 1980s, Dr Paul Sugarbaker introduced the ‘Sugarbaker procedure’ for peritoneal mesotheliomas, wherein heated chemotherapeutic drugs were directly applied to the abdomen after surgically removing any visible tumours. 1 Since then Cytoreductive surgery (CRS) with hyperthermic intraperitoneal chemotherapy (HIPEC) is indicated as treatment for these neoplasms. It consists of almost complete removal of the peritoneal surface, multiple visceral resections, a variable number of intestinal anastomosis, followed byperfusion of chemotherapy inside the abdominal cavity, for 90 min at 42 °C.2,3

The wide extent of surgical resection and physicochemical trauma of the HIPEC alters capillary permeability, resulting in tissue damage and facilitating abdominal and systemic complications with postoperative morbidity and mortality ranging from 22 to 41 % and from 2 to 5 % respectively, with a significant increase in ICU stay and hospitalization time. 4, 5

Also, cytoreductive surgery is usually associated with significant fluid shift attributable to suboptimal nutritional status, prolonged preoperative starvation, intraoperative blood and fluid loss, pharmacological vasodilation by neuraxial (epidural) and systemic anaesthetic drugs, intraoperative evaporative loss and the vasodilation due to systemic inflammatory response to surgery (SIRS) resulting in hypotension and altered hemodynamics in the intra-operative and immediate post-operative settings. So, there is need for rigorous hemodynamic monitoring and appropriate fluid therapy in the perioperative period. Permissive infusion regimen was proposed in the past 6, 7to counteract fluid, blood, and protein losses; however, it excessively exposes the patient to the risk of fluid overload, tissue edema, and severe abdominal complications. On the other hand, the use of restrictive infusional regimens may expose the patient to hemodynamic instability, detrimentaltissue hypoperfusion, organ damage, and worsen the nephrotoxic chemotherapy drug effect. Different markers of global perfusion are serum lactate, mixed and central venous oxygen saturation (ScvO2), Co2 gap in between central venous and arterial blood, (P v-a CO2), left ventricular strain and markers of local perfusion are temperature gradient (Tc-toe), skin mottling, capillary refill time, peripheral perfusion index (PPI), tissue oxygen saturation (Sto2) and transcutaneous oxygen measurement (Ptco2). 8

The current standard of care in our centre Institute rotary cancer hospital (IRCH) has been a fluid therapy guided by clinical parameters. Although there is strong evidence supporting goal-directed approach (using Flotrac/Vigileo system) to perioperative fluid therapy in case of major abdominal surgeries, leading to significant reduction of systemic complications and enhanced recovery 9-11, there is no concrete evidence for CRS/HIPEC surgery. So, we would like to conduct the proposed study to findout the optimal fluid management strategy in CRS/HIPEC. Primary end points will be serum NGAL levels. Secondary end pointswill be serum lactate levels (surrogate marker of tissue perfusion) intraoperatively and post operatively, incidence of renal complications (defined by AKIN criteria), length of ICU stay (till fit to discharge based on ICU physician discretion) and 30-day mortality.

Preliminary work done if any: The present topic is new and not much researched worldwide. PI has done an extensive review and found gap in knowledge and lack of existing trials evaluating the type of fluid therapy protocol on incidence of acute kidney injury in patients undergoing CRS/HIPEC surgery. Also, till date serum NGAL levels as biomarker for AKI in CRS/HIPEC surgery has not been evaluated before. Considering the novelty of the topic and overall need for such research we strongly believe that the results of this study would be beneficial to population at large.

The relevance and expected outcome of the proposed study: Patients undergoing CRS/HIPEC surgery are prone to develop acute kidney injury in the post- operative period due to various factors such as use of chemotherapeutic agent (cisplatin) as well as due to hemodynamic fluctuations happening throughout the surgery. Although there is strong evidence supporting goal-directed approach (using Flotrac/Vigileo system) to perioperative fluid therapy in case of major abdominal surgeries, leading to significant reduction of systemic complications and enhanced recovery, there is no concrete evidence for CRS/HIPEC surgery. Through this study we will be able to assess and compare the institutional fluid therapy protocol versus goal directed fluid therapy protocol in patients undergoing CRS/HIPEC surgery and see the effect of goal-directed therapy on post-operative neutrophil gelatinase-associated lipocalin. Also, we will compare length of ICU stay and 30-day mortality.

Aim: This study is aimed to assess whether the use of Goal directed fluid therapy protocol is associated with significant change in perioperative outcomes compared to standard institutional fluid therapy protocol guided by clinical parameters in patients undergoing cytoreductive surgery with hyperthermic intraperitoneal chemotherapy.

 
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