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CTRI Number  CTRI/2023/08/057089 [Registered on: 30/08/2023] Trial Registered Prospectively
Last Modified On: 26/08/2023
Post Graduate Thesis  Yes 
Type of Trial  Observational 
Type of Study   Cohort Study 
Study Design  Other 
Public Title of Study   Understanding the Link Between Stress Hormones and Heart Changes in Patients on Steroids During Pituitary Surgeries: An Observational Study 
Scientific Title of Study   Prospective observational study on the association between perioperative cortisol level and hemodynamic variables in patients on steroid therapy undergoing pituitary surgeries 
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 Unnikrishnan P 
Designation  Additional Professor 
Affiliation  Sree Chitra Tirunal Institute for Medical Sciences and Technology 
Address  Division of Neuroanaesthesia, Department of Anaesthesia, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram.

Thiruvananthapuram
KERALA
695011
India 
Phone  9447662321  
Fax    
Email  drunniz@sctimst.ac.in  
 
Details of Contact Person
Scientific Query
 
Name  Dr Unnikrishnan P 
Designation  Additional Professor 
Affiliation  Sree Chitra Tirunal Institute for Medical Sciences and Technology 
Address  Division of Neuroanaesthesia, Department of Anaesthesia, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram.

Thiruvananthapuram
KERALA
695011
India 
Phone  9447662321  
Fax    
Email  drunniz@sctimst.ac.in  
 
Details of Contact Person
Public Query
 
Name  Dr Praveen R S 
Designation  DM NeuroAnaesthesia Resident 
Affiliation  Sree Chitra Tirunal Institute for Medical Sciences and Technology 
Address  Division of Neuroanaesthesia, Department of Anaesthesia, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram.

Thiruvananthapuram
KERALA
695011
India 
Phone  7598125517  
Fax    
Email  praveensarguru@gmail.com  
 
Source of Monetary or Material Support  
Sree Chitra Tirunal Institute for Medical Sciences and Technology, Jai Nagar W Rd, Chalakkuzhi, Medical college (p.o), Thiruvananthapuram, Kerala-695011 
 
Primary Sponsor  
Name  Intramural Funds, Sree Chitra Tirunal Institute for Medical Sciences and Technology 
Address  Jai Nagar W Rd, Chalakkuzhi, Medical college (p.o), Thiruvananthapuram, Kerala  
Type of Sponsor  Government medical college 
 
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 Unnikrishnan P  Sree Chitra Tirunal Institute for Medical Sciences and Technology  Neurosurgical operation theatre and ICU, 4th floor, Neuro block,SCTIMST, Jai Nagar W Rd, Chalakkuzhi, Medical college (p.o),Trivandrum,Kerala- 695011
Thiruvananthapuram
KERALA 
9447662321

drunniz@sctimst.ac.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee,Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum  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  nil  nil 
Comparator Agent  nil  nil 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  1.Consenting adult patients undergoing surgery for pituitary tumours at Sree Chitra
Tirunal Institute for Medical Sciences and Technology
2.ASA (American Society of Anaesthesiologists) class 1,2 and 3
3.GCS 15/15 prior to the surgery 
 
ExclusionCriteria 
Details  1.Patient refusal
2.Age less than 18 years, more than 60 years
3.Emergency surgery
4.Patients with Cushing disease, previous history of adrenal insufficiency
5.ASA class 4,5 patients
6.Patients needing steroid supplementation due to other diseases
7.Pregnant and lactating mothers  
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To assess the correlation between perioperative
cortisol levels and hemodynamic variables in patients on steroid therapy undergoing
pituitary surgeries 
Serum cortisol level will be measured Baseline day before surgery
7:30 am on the day of surgery
after induction
after sphenoid drilling
during hypotensive episode 
 
Secondary Outcome  
Outcome  TimePoints 
To find the influence of serum cortisol level & steroid therapy, on hemodynamic variables (including episodes of unexplained hypotension,
maximum fall in MAP & hypertension) & the incidence of dyselectrolytemias in patients undergoing pituitary surgeries for tumour resection 
Hemodynamic variables will be recorded in 10 minute intervals during intraoperative period. Electrolyte & serum lactate level will be measured after induction and
at the end of surgery 
 
Target Sample Size   Total Sample Size="90"
Sample Size from India="90" 
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)   04/09/2023 
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   N/A 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary  

Patients will be recruited from the elective operating list of the neurosurgery department. The Principal Investigator will study the procedure and screen for inclusion and exclusion criteria. Written informed consent will be obtained if the participant is eligible for inclusion. Consenting patients will be included in the study protocol.  

A preoperative baseline heart rate (H.R.), blood pressure (B.P.) and baseline serum cortisol (S.C. Baseline) value will be obtained as part of the pre-anaesthetic evaluation, during the first meeting of the anaesthesiologist with the patient. Baseline demographics, hormonal profile, size and type of lesion based on preoperative MRI will be noted. The same preanesthetic preparation as per institutional protocol will be given to all the patients.  

On the day of the surgery, a serum cortisol sample will be obtained at 7:30 AM (SC 1). The same perioperative steroid therapy as per the institutional protocol will be given to all patients on the day of surgery. The steroid dose and timing of administration will be noted. Then the patient will be shifted to the operating room.Anaesthesia protocol will be standardized for all the patients included in the study.Under Lignocaine (2%), skin infiltration I.V. access will be obtained. The hemodynamic parameters: H.R. and B.P. will be noted. Patients will be preoxygenated for 3 minutes with FiO2 of 1.0 at a flow rate of 10L/min. Then the patient will be induced with fentanyl 2mcg/kg and propofol 2-3 mg/kg, targeted to attain a BIS value of 45-55, and vecuronium 0.1 mg/kg will be given after confirming mask ventilation and proceed with intubation. The patient will be mechanically ventilated in volume control ventilation (VCV) mode with a tidal volume of 6-8 ml/kg and minute ventilation (Mv) adjusted to maintain an ETCO2 of 35mm of Hg. Post intubation, Invasive Blood Pressure (IBP) with Pulse Pressure Variability (PPV) monitoring also will be established, and fluid deficit denoted by PPV >12 will be corrected. Serum cortisol (SC2) and an Arterial Blood Gas (ABG) analysis sample with serum lactate value will be sent. Anaesthesia will be maintained using a combination of Oxygen/Air (FiO2 0.5) and sevoflurane to maintain a MAC above 0.7, with a BIS target of 45-55, along with an infusion of atracurium of 0.06mg/kg/hour and fentanyl 1microgram/kg/hour. H.R., B.P. and PPV will be monitored continuously and noted every 10 minutes during the intraoperative period. A serum cortisol sample will be sent intraoperatively after the sphenoid drilling (SC3) to check for the hormonal profile after the period of maximum surgical stimulation. 

Unexplained hypotension will be defined as hypotensive episodes (a 20% fall in mean arterial pressure (MAP) from the baseline) lasting for >3 minutes and refractory to fluid administration and due to reasons other than sepsis, anaphylaxis, neurogenic, myocardial ischemia, venous air embolism, arrhythmias, hypovolemia or haemorrhage (Hypotension-X), which will be recorded with the time of occurrence and a serum cortisol sample (SC-X) will be sent during one such episodes, if any. Similarly, Hypertensive episodes (a 20% elevation in mean arterial pressure from baseline) will be marked as hypertension (HTN) and will be recorded with accompanying interventions, if any (e.g., adrenaline infiltration and iatrogenic changes in blood pressure for checking hemostasis). HTN, without any vasopressor stimulus or neural reflex, will be considered a pain stimulus and treated with 1 mcg/Kg bolus of Fentanyl. The maximum fall in MAP will also be noted. The maximum fall in MAP is defined as the baseline MAP before the induction minus the minimum MAP during the intraoperative period.  

The total volume of crystalloids and colloids used will be noted separately. The total cumulative dose of vasopressors (Mephentermine, Phenylephrine and Noradrenaline) will also be recorded separately at the end of the surgery. 

ABG with serum lactate will be sent at the end of the surgery. Incidence of postoperative complications like diabetes insipidus or hyponatremia in the immediate postoperative period also will be recorded. 

 

 
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