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CTRI Number  CTRI/2025/08/092934 [Registered on: 12/08/2025] Trial Registered Prospectively
Last Modified On: 09/08/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Other (Specify) [Administration of calories based on diaphragm thickness]  
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   Study of benefits of restricted feeding vs overfeeding in patients admittted in ICU and their outcomes 
Scientific Title of Study   Outcome of calorie titration based on diaphragmatic excursion in mechanically ventilated ICU Patients a prospective randomized controlled trial. 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Mukund Sajjan 
Designation  Senior resident 
Affiliation  All Institute of Medical Sciences,Jodhpur 
Address  Department of Anaesthesiology and Critical care,All India Institute of Medical Sciences,HI Area Phase II,Basni Jodhpur,Rajasthan 342005 India
.
Jodhpur
RAJASTHAN
342005
India 
Phone  9786171500  
Fax    
Email  sajju.sj@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Mukund Sajjan 
Designation  Post graduate in DM Critical care medicine 
Affiliation  All Institute of Medical Sciences,Jodhpur 
Address  Department of Anaesthesiology and Critical care,All India Institute of Medical Sciences,HI Area Phase II,Basni Jodhpur,Rajasthan 342005 India
.
Jodhpur
RAJASTHAN
342005
India 
Phone  9786171500  
Fax    
Email  sajju.sj@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Mukund Sajjan 
Designation  Senior resident 
Affiliation  All Institute of Medical Sciences,Jodhpur 
Address  Department of Anaesthesiology and Critical care,All India Institute of Medical Sciences,HI Area Phase II,Basni Jodhpur,Rajasthan 342005 India
.
Jodhpur
RAJASTHAN
342005
India 
Phone  9786171500  
Fax    
Email  sajju.sj@gmail.com  
 
Source of Monetary or Material Support  
All India Instititute of medical sciences, Jodhpur, Rajasthan, 341001, India 
 
Primary Sponsor  
Name  All Institute of Medical SciencesJodhpur 
Address  Department of Anaesthesiology and critical care,AIIMSJodhpur,Rajasthan, 342001, India 
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 
Drmukund sajjan  Aiims Jodhpur  Department of Anaesthesiology and Critical care, Aiims Jodhpur, rajasthan 342005,India
Jodhpur
RAJASTHAN 
09786171500

sajju.sj@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
AIIMS JODHPUR  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: J22||Unspecified acute lower respiratory infection,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Standard fixed amount of calories administration for nutrition in Icu patients who are mechanically ventilated  Addition of fixed amount of calories will be compared to the titrated administration of calories in patients during the course of mechanical ventilation and will be monitored their outcome 
Intervention  Titrated supplement of nutrition  addition of titrated Ryles tube feed based on diaphragm thickness and excursion monitered by Ultrasound in mechanically ventilated patients in ICU 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  70.00 Year(s)
Gender  Both 
Details  Mechanically ventilated patients in view of altered sensorium 
 
ExclusionCriteria 
Details  Refusal of informed consent
Known case of phrenic nerve injury
Patients with chest trauma, abdominal trauma
Patients with pathologies related to increased abdominal pressure
Patients with neuromuscular muscular diseases
Continuous infusion of muscle-paralyzing agents
abnormal values of myocardial and muscular damage markers at ICU admission,
presence of thoracotomy, pneumothorax or pneumo-mediastinum, pregnancyPatients with previous history of delirium
 
 
Method of Generating Random Sequence   Random Number Table 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Weaning of mechanically ventilated patients between titrated calorie administration during the initial 1 week and fixed calorie administration during the 1 st week in mechanically ventilated patients in ICU  Weaning of mechanically ventilated patients between titrated calorie administration during the initial 1 week and fixed calorie administration during the 1st week in mechanically ventilated patients in Icu 
 
Secondary Outcome  
Outcome  TimePoints 
To assess diaphragm thickness at 1st week
serum phosphate level at days 0,3 & 7th day
IL-6 marker of oxidant injury on day 7
Difficulty in weaning from mechanical ventilator after 1 week of ventilation
To assess the efficacy & outcome of patients who undergo graded increase in nutrition over 1 month
To assess the efficacy & outcome of patients who undergo graded increase in nutrition
To assess the Gastrointestinal issues
Imbalance of hyperglycemia events 
To assess diaphragm thickness at 1st week
serum phosphate level at days 0,3 & 7th day
IL-6 marker of oxidant injury on day 7
Difficulty in weaning from mechanical ventilator after 1 week of ventilation
To assess the efficacy & outcome of patients who undergo graded increase in nutrition over 1 month
 
 
Target Sample Size   Total Sample Size="72"
Sample Size from India="72" 
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)   30/08/2025 
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="6"
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  

Our study focuses on trying to  avoid the detrimental effects of overfeeding and underfeeding with the concept that in patients with lower diaphragm excursion less supplementation of the calorie will result in lower amount of overfeeding complications such as less oxidative stress and less free radical generation and less workload of the lungs  and will put less stress in the respiratory system and thereby avoiding diaphragm dysfunction , organ failure from insulin resistance endogenous hyperglycemia and free radical injury

Rationale of the study supported by cited literature

Diaphragm dysfunction, measured by Diaphragm excursion are correlated with MNUTRIC scores indicated as an indirect marker of malnutrition , and its efficacy in prevention of overfeeding and underfeeding complications in ICU patients and its role in weaning outcome from mechanical ventilation

HypothesisWe hypothesize that calorie adjustment based on diaphragm excursion during the initial 1 week  prevent the consequences of overfeeding and underfeeding  complications in critically ill patients as malnutrition are associated with significant diaphragm dysfunction in critically ill patients  .

Research questionsDoes calorie titration based on diaphragm excursion prevent the complications of overfeeding and underfeeding in mechanically ventilated ICU patients.

Aim To prove that calorie titration based on diaphragm excursion overcomes the effects of underfeeding or overfeeding complications in mechanically ventilated ICU patients

PRIMARY OBJECTIVE Weaning of mechanically ventilated patients between  titrated calorie administration during the initial 1 week  and fixed calorie administrat

SECONDARY OBJECTIVES

to assess diaphragm thickness, diaphragm excursion in all the groups.

Serum phosphate level in prevention of refeeding syndrome and consequent diaphragmatic dysfunction

 IL-6 a marker of oxidant injury among both groups

 Difficulty in weaning from the mechanical ventilator

To assess the efficacy and outcome of patients who undergo graded increase in nutrition and its effects of overcoming the abrupt transition of overfeeding vs underfeeding states in critically ill patients

 To assess the Gastrointestinal intolerances among both groups

 Incidence of hyperglycemia events among both groups (Blood glucose>180)

Detailed methodology

This is a single center prospective randomized  controlled study

  Patients  fulfilling  inclusion criteria will be randomly allocated into two groups and allocation concealed using sealed envelope method. 

GROUP A  Mechanically ventilated patient undergoing  calorie titration based on  diaphragm excursion velocity

      GROUP B Mechanically ventilated patients undergoing fixed   25kcals/kg/day

    The study will be conducted in mechanically ventilated patients of acute hypoxic respiratory failure patient  for the first day of intubation to 5 th day of intubation

Ultrasound imaging of diaphragmatic excursion velocity  will be assessed in mechanically ventilated patients at a pressure support of 5 cm H2O of group A and will be fed accordingly

 Excursion  of less than 1 cm_ 10 kcals/kg

  Excursion  of 1-2 cm-   20kcals/kg

  Excursion  of  2-3cm-30kcals/kg

  GroupB Group B will be fed with usual 25kcals/kg

Patients will be randomized into two groups , group A and group B, who are undergoing mechanical ventilation and from the day one of intubation their calorie feeds will be delivered according to the above protocols for the respective groups , There is no titration of protein calories and it is given at 1.3 gm to 1.5 gm/kg among both the groups.

Usg diaphragm assessment will be done with the help of linear and phased array probe and diaphragm thickness fraction and diaphragm excursion  will be calculated among both the groups on a daily basis and noted

Day 5 th diaphragm thickness fraction and Diaphragm excursion  will be taken as the final reading for the primary objective assessment

Diaphragm thickness will be assessed with the help of linear probe at the zone of opposition by keeping the linear probe parallel to the anterior axillary line and putting the M mode across the zone of opposition and calculating the diaphragm thickness, with the normal range being above 30 %

Diaphragm excursion  will be calculated with the help of phased array probe placed at the subcostal level and placing the M mode along the diaphragm excursion and calculating its excursion  with the normal range between 1-2 cm

These measurements are made at the level of pressure support of 5 cm in spontaneous pressure support mode of ventilation

Baseline routine investigations consisting of Complete blood count, Renal function test, Liver function test, Procalcitonin , D-dimer parameters will be recorded among the two groups

Serum phosphate level on day 2 will be assessed among the both groups and complications and incidence of refeeding syndrome will be monitored

Random blood glucose monitoring ( 4 readings /day) for the 5 days will be taken into account, Rbs of more than 180 will be considered as hyperglycemia and Rbs of < 70 will be considered as Hypoglycemia

Diarrhea/Abdominal pain /Constipation episodes , and any other symptoms of gastro intolerance will be documented among both groups

Baseline vasopressor support, single reading of  vitals on day 1 to day 5 will be documented

Patients undergoing high amounts of hemodynamic instability such as refractory vasopressor support, MAP < 65 will be excluded from the study

Dieticians help will be obtained for the administration of calculated amount of calories and advice will be followed

Renal, hepatic, diabetic diet will be followed and be administered based on the amount of calorie as per the protocol

 Inclusion criteria

 

Age>18

Mechanically ventilated patients in ICU  in view of respiratory distress/altered sensorium

 Exclusion criteria

       Refusal of informed consent

         Known case of phrenic nerve injury

        Patients with chest trauma, abdominal trauma

         Patients with pathologies related to increased abdominal pressure

         Patients with neuromuscular muscular diseases

         Continuous infusion of muscle-paralyzing agents 

         

         presence of thoracotomy, pneumothorax or pneumo-mediastinum, pregnancy

 

Sampling population Patient admitted to ICU who satisfy the inclusion criteria

Sample size of our study is calculated on basis of a study done by Yifei Wang et al on impact of early high protein intake in critically ill patients ,a RCT, where the Mechanical ventilation duration mean days were found to be 9 vs 10.25 in the test and reference group

Assuming a pooled standard deviation of 1.88

Sample size for each group is found to be 36 in each group

Hence  2 groups  comprising a total sample size of 72 is obtained

To achieve a power of 80 %

And a level of significance of 5%

Sample size is calculated by using by Two independent means formula


 

Data analysis plan: Data will be collected using google form.

Statistical analysis of the data will be performed using SPSS Latest version available.

The Q-Q plot will be used to understand the distribution of continuous outcome variables.

Continuous variables will be expressed as mean ± standard deviation/ Median (IQR)  depending on its distribution and categorical variable as frequency (percentage).

Comparisons will be performed by one-way analysis of variance (ANOVA) followed by Tukey’s Post-hoc test for normally distributed or  Kruskal–Wallis test for non-normally distributed, and chi-square test of association for categorical variables.

A p-value of < 0.05 will be considered to be statistically significant.

 


 
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