| 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
|
|
|
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
|
|
|
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. |