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CTRI Number  CTRI/2021/06/034152 [Registered on: 10/06/2021] Trial Registered Prospectively
Last Modified On: 09/06/2021
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug
Surgical/Anesthesia 
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   Effect of high oxygen level in body on body functions after surgery in old aged patients 
Scientific Title of Study   Effect of increased Intraoperative systemic oxygen delivery on postoperative outcomes in elderly patients undergoing major abdominal surgery- A Randomized controlled trial  
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Kishore kumar M 
Designation  Junior resident 
Affiliation  JIPMER 
Address  Department of Anesthesiology and critical care,Old hospital block, second floor,JIPMER, Puducherry

Pondicherry
PONDICHERRY
605006
India 
Phone  7904282047  
Fax    
Email  kkishore576@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Ajay Kumar Jha 
Designation  Assistant Professor 
Affiliation  JIPMER 
Address  Department of Anesthesiology and critical care,SSB Annex block,JIPMER, Puducherry

Pondicherry
PONDICHERRY
605006
India 
Phone  9868477642  
Fax    
Email  drajaykjha@rediffmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Ajay Kumar Jha 
Designation  Assistant Professor 
Affiliation  JIPMER 
Address  Department of Anesthesiology and critical care,SSB Annex block,JIPMER, Puducherry

Pondicherry
PONDICHERRY
605006
India 
Phone  9868477642  
Fax    
Email  drajaykjha@rediffmail.com  
 
Source of Monetary or Material Support  
Intra mural Fund, Dean Research office ,First floor,Administrative Block,JIPMER,Dhanvantari Nagar,Pondicherry-605006 
 
Primary Sponsor  
Name  Intramural FundingJIPMER 
Address  Dean(Research)First floor,Administrative Block,JIPMER,Dhanvantari Nagar,Pondicherry-605006 
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 Kishore kumar M  JIPMER  Jawaharlal Institute of Postgraduate Medical Education and Research,Emergency and trauma block, JIPMER Campus Rd, Gorimedu, Dhanvantari Nagar, Puducherry, 605006.
Pondicherry
PONDICHERRY 
7904282047

kkishore576@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
JIPMER IEC  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: O||Medical and Surgical,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Intervention Arm  Intervention arm (Maintenance of central venous oxygen saturation of ≥75%) Central venous oxygen saturation will be augmented by maintaining mean arterial pressure between 90 -105 mm Hg by continuous and variable dose of iv noradrenaline infusion initially at 0.05mcg/kg/min at the maximum of 0.1mcg/kg/min during the intraoperative period and the dose of noradrenaline will be reduced once we reach mean arterial pressure of 90mm Hg followed by a higher fractional inspired oxygen (Fio2) 
Comparator Agent  Standard Care Arm  Standard care arm Central venous oxygen saturation will be monitored and intraoperative care, and blood pressure target will be decided by attending anesthesia team.  
 
Inclusion Criteria  
Age From  60.00 Year(s)
Age To  90.00 Year(s)
Gender  Both 
Details  1.Age more than 60 years
2.American Society of Anesthesiologists (ASA) physical status I, II and III
3.Patient undergoing elective and emergency major abdominal surgery of any indication lasting more than two hours and/or expected blood loss >500 ml
 
 
ExclusionCriteria 
Details  1. Patient already receiving mechanical ventilation
2.Patient already receiving inotrope
3.Poorly controlled hypertension
4 Contra indication to IJV catheterization
5. Planned reoperation within 3 months
6.Preoperative immobility or inability to walk unaided
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
To assess the effect of higher systemic oxygen delivery on composite of death, major postoperative complications compared to the standard care  Post op day 1, day before discharge,After 3 month 
 
Secondary Outcome  
Outcome  TimePoints 
1. To assess the effect of increased systemic oxygen delivery on length of hospital stay compared to standard care
2. To assess the effect of increased systemic oxygen delivery on postoperative quality of life compared to standard care
3.To assess the effect of increased systemic oxygen delivery on cvs,rs,cns,renal and GIT system compared to standard care
 
Post op day 1, day before discharge,After 3 month  
 
Target Sample Size   Total Sample Size="150"
Sample Size from India="150" 
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)   01/07/2021 
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="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   nil 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary  

Major abdominal surgery predisposes elderly patients to increased risk of morbidity and mortality. They experience variety of complications that affect every system of the body like transient ischemic attack, stroke, cognitive dysfunction, postoperative Myocardial infarction, pulmonary embolism, acute kidney injury, renal failure requiring dialysis, intraabdominal sepsis, delayed return of bowel function, and prolonged mechanical ventilation,Intraoperative hemodynamic fluctuations, blood loss, fluid shift, electrolyte imbalances and increased duration of surgery are known to affect postoperative outcomes. Systemic oxygen delivery to vital organs may be compromised during intraoperative hypotension, anemia, fluid overload induced oedema. Additionally, elderly has multiple comorbid illnesses and these illnesses put them at the risk of impaired oxygen delivery due to macro and micro vessel atherosclerosis and dysfunction. Intraoperative hypotension may further compromise systemic oxygen delivery. Ensuring a higher systemic oxygen delivery by avoiding hypotension and higher oxygenation might reduce the incidence the postoperative morbidity and mortality.Hypotension and hemodynamic fluctuations during intraoperative period may compromise systemic oxygen delivery. In addition, elderly patients have multiple comorbid illness and suboptimal physiologic reserve atherosclerotic burden that can reduce oxygen delivery to major organs. Therefore, improvement in tissue oxygen delivery by augmenting cardiac output, systemic blood pressure and increased oxygenation would ensure better intraoperative metabolic mileu in vital organs. Central venous oxygen saturation (ScvO2) is known as a surrogate of systemic oxygen delivery and systemic oxygen consumption.  ScvO2 monitoring is a feasible option during intra operative period to ensure systemic oxygen delivery. Direct systemic oxygen delivery calculation appears challenging during intraoperative period because the metabolic oxygen consumption using Lafarge equation may not be valid during anesthesia. Furthermore, monitoring of mixed venous oxygen saturation requires pulmonary artery catheterization.Central venous oxygen saturation monitoring during intraoperative period in elderly patients undergoing major abdominal surgery may provide a comprehensive indicator of intraoperative hypotension, systemic oxygen delivery, and oxygen consumption and it would help in ensuring protection of vital organs. Maintaining central venous oxygen saturation at a higher cut-off by eliminating hemodynamic fluctuations and ensuring proper oxygenation by both inotropic agent and supplemental oxygenation is expected to improve postoperative outcomes.

After obtaining approval from Department postgraduate research monitoring committee, Institute ethics committee and completing CTRI registration, patients satisfying eligibility criteria will be included in this study. Written informed consent explaining about the procedure, risks and any adverse events will be obtained from the patients before being enrolled into the study. Enrollment and consent will be preferably obtained a day to prior to surgery. The patient will be enrolled in 1:1 ratio. Relevant demographic data and investigation details will be obtained from the case sheet.

Anesthetic management: On arrival standard monitors, i.e. pulse oximetry (SpO2), non-invasive blood pressure, 5 lead electrocardiography (ECG) will be connected. A wide bore iv cannula will be inserted and fluid (Ringer lactate @ 5ml/kg) will be infused before induction of anesthesia. Regional anesthesia technique, choice and dosage of local anesthetic agent will be decided by the attending anesthesia team. Bispectral index (BIS) will be attached before induction of anesthesia.Anesthesia induction will begin with preoxygenation for a minimum of 3 minutes and will be achieved by inj. Fentanyl (2 mcg/kg), thiopentone (4-5 mg/kg) and rocuronium (1 mg/kg). BIS will be maintained between 40-60. Hypotension and hypertension during induction will be managed by boluses of noradrenaline (1mcg/kg) and esmolol (0.5 mg/kg), respectively. Maintenance of anesthesia will be preferably done using Isoflurane (variable dial settings) in FiO2 (40-80% with air) and supplemental fentanyl boluses (0.5 mcg/kg) to maintain BIS between 40-60. Ventilator settings will be adjusted to maintain End tidal carbon dioxide (ETCO2) between 35-45 mm Hg. Initially FiO2 will be kept at 0.4.  After induction of anesthesia, central venous catheter will be placed in the right internal jugular vein under aseptic precaution. The arterial cannula will be secured in left radial artery and will be connected to a pressure transducer.

INTERVENTION ARM     Study will commence once patient positioning is achieved post intubation and all   monitoring devices are in place. Baseline hemodynamic data will be recorded and   repeated at 30 minutes interval. Fluids will be infused at the rate of 5 ml/kg/hr in open abdominal surgery and 3ml/kg/hour in laparoscopic surgery. Hemoglobin will be maintained > 8 gm/dl and PRBC will be transfused accordingly. Blood loss will be replaced with crystalloid, colloid or PRBC in 1:3 and 1:1 ratio. Baseline central venous oxygen saturation (ScVo2) will be obtained after patient positioning. If the baseline ScVo2 < 75% or if it falls to < 75% during surgery, we will follow a specific treatment protocol mentioned in annexure I. We will measure ScvO2 again 30 minutes after intervention. Thereafter, we will measure ScvO2 every 2 hourly.

STANDARD CARE ARM Baseline central venous oxygen saturation will be measured, and the value is monitored every two hours till the end of surgery. Remaining intervention including fluid management, regional anesthesia, anesthetic agents will be left according to the attending anesthesiologist team. However, BIS will be maintained between 40-60.

Intraoperative blood sugar will be maintained between 100-200 mg/dl. Intraoperative temperature will be kept between 36-370C with the help of prewarmed fluid and external body warming devices.

On the day of surgery, data concerning the performed procedure will be collected, including duration of surgery, total fluid administration, central venous oxygen saturation, norepinephrine dosage, FiO2, urine output, hemodynamic parameters, blood loss, type of surgery and type of surgical access (open vs. laparoscopic). Furthermore, data regarding number and types of abdominal drains, nasogastric tubes, urinary catheters, and postoperative analgesic will be collected

1st postoperative day

All postoperative outcomes will be assessed according to the defined criteria. Additionally, we will collect all investigation data from the case sheet of the patient. Hemodynamic parameter, urine output, fluid balance, transfusion requirement will also be collected.

Postoperative visit 1 day before discharge

Fluid balance, postoperative outcomes as defined will be collected from the case sheet, investigation, Chest Xray, EQ-5DL filled questionnaire will be collected. Postoperative outcomes assessors will be blinded to study randomization arm. All uncertainty related to outcomes will be resolved with the help of neurologist, cardiologist, radiologist and surgeons. 

After 3 months EQ-5DL filled questionnaire will be collected from patient either in person or over telephone.

Outcome Definitions

 CVS COMPLICATIONS Perioperative myocardial infarction reflected by changes in electrocardiography like ST segment changes, new onset pathological q wave, any new onset bundle branch block, atypical chest pain, persistent hypotension less than 90 mm Hg, requirement of inotrope, elevated Troponin-T or any incidence of percutaneous coronary intervention

NEUROLOGICAL COMPLICATIONS Stroke ( neurological deficit attributed to an acute focal injury of the central nervous system (CNS) by a vascular cause, including cerebral infarction, intracerebral hemorrhage (ICH), and subarachnoid hemorrhage (SAH)) ,transient ischemic attack ( transient episode of neurologic dysfunction due to the focal brain, spinal cord, or retinal ischemia, without acute infarction or tissue injury), delirium (transient, usually reversible, cause of mental dysfunction and manifests clinically with a wide range of neuropsychiatric abnormalities guided by MOCA score)

PULMONARY COMPLICATIONS Respiratory failure (room air oxygen saturation <90%, supplemental oxygen requirement to maintain saturation >94%, mechanical ventilation, reintubation) pulmonary edema, any chest radiograph evidence of consolidation, ARDS satisfying Berlin Criteria

RENAL COMPLICATIONS Any rise in creatinine more than 0.3mg/dl or 50%from baseline and requirement of dialysis or renal replacement therapy

GASTROINTESTINAL COMPLICATIONS Evidence of postoperative abdominal distension, Delayed return of bowel sounds (postoperative days), wound infection

QUALITY OF LIFE Quality of life will be assessed based on EQ5D3L scale before hospital discharge and after 3months either in person or over telephone


 
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