FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
CTRI Number  CTRI/2025/08/092159 [Registered on: 01/08/2025] Trial Registered Prospectively
Last Modified On: 31/07/2025
Post Graduate Thesis  Yes 
Type of Trial  Observational 
Type of Study   Cross Sectional Study 
Study Design  Other 
Public Title of Study   Comparison of serum free carnitine levels in children (6 month-59 months) with Moderate and Severe Acute Malnutrition as compared to children with normal nutrition 
Scientific Title of Study   Serum Carnitine Levels in under five children with Moderate and Severe Acute Malnutrition 
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 Nilofer Khan 
Designation  Post graduate Resident  
Affiliation  UCMS and GTB Hospital 
Address  MCH IVth Floor, Pediatrics Ward Department of Pediatrics, University College of Medical Sciences and GTB Hospital, Delhi
Department of Pediatrics, MCH 6th Floor, University College of Medical Sciences and GTB Hospital, Delhi
New Delhi
DELHI
110095
India 
Phone  9651014321  
Fax    
Email  niloferkhan951@yahoo.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Sumaira Khalil 
Designation  Associate Professor 
Affiliation  UCMS and GTB Hospital 
Address  Room No. 601, MCH 6th Floor, MCH Building, University College of Medical Sciences and GTB Hospital, Delhi
Department of Pediatrics, Pediatric Ward, 4th Floor, MCH Building, GTB Hospital, Delhi
East
DELHI
110095
India 
Phone  9810424664  
Fax    
Email  skhalil@ucms.ac.in  
 
Details of Contact Person
Public Query
 
Name  Dr Sumaira Khalil 
Designation  Associate Professor 
Affiliation  UCMS and GTB Hospital 
Address  Room No 601, MCH 6th Floor, MCH Building, University College of Medical Sciences and GTB Hospital, Delhi
Department of Pediatrics, Pediatric Ward, 4th Floor, MCH Building, University College of Medical Sciences and GTB Hospital Delhi
East
DELHI
110095
India 
Phone  9810424664  
Fax    
Email  skhalil@ucms.ac.in  
 
Source of Monetary or Material Support  
Intramural Research Grant, University College of Medical Sciences, Dilshad Garden, Delh 110095 
 
Primary Sponsor  
Name  Intramural Research Grant University College of Medical Sciences 
Address  UCMS, Dilshad Garden, Delhi 110095 India 
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 Nilofer Khan   University College of Medical Sciences and GTB Hospital  Department of Pediatrics, 6th Floor MCH building, University College of Medical Sciences and GTB Hospital Delhi
East
DELHI 
9651014321

niloferkhan951@yahoo.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee and Human Research UCMS   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: E440||Moderate protein-calorie malnutrition, (2) ICD-10 Condition: E43||Unspecified severe protein-caloriemalnutrition,  
 
Intervention / Comparator Agent  
Type  Name  Details 
 
Inclusion Criteria  
Age From  6.00 Month(s)
Age To  59.00 Month(s)
Gender  Both 
Details  Cases
Group 1: Children aged between 6 months-59 months with moderate acute malnutrition (weight for length/height Z-score between -3 to -2 and/or mid-upper-arm circumference between 11.5-12.5 cm)
Group 2: Children aged between 6 months-59 months with moderate acute malnutrition (weight for length/height Z-score between less than -3Z and/or mid-upper-arm circumference between less than 11.5)
Comparison Group: Children aged between 6 months-59 months with no undernutrition (weight for length/height Z-score between -1 to +1 and/or mid-upper-arm circumference more than 12.5 cms) 
 
ExclusionCriteria 
Details  1. Children with suspected or confirmed inborn error of metabolism or primary carnitine
deficiency
2. Children on carnitine supplementation
3. Children with confirmed or suspected chronic kidney, chronic liver disease cardiomyopathy congenital heart disease and congenital malformation 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Serum free carnitine levels  at Baseline 
 
Secondary Outcome  
Outcome  TimePoints 
1. proportion of children with carnitine deficiency
2. proportion of children with carnitine insufficiency
3. correlate with lipid profile, total protein and serum albumin
4. correlate with age, gender, weight for height and mid upper arm circumference 
at Baseline  
 
Target Sample Size   Total Sample Size="120"
Sample Size from India="120" 
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)   15/08/2025 
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="4"
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   Title: Serum Carnitine Levels in Under-Five Children with Moderate and Severe Acute
Malnutrition
Aim: To determine and compare serum free carnitine levels in children (6 month-59 months) with
Moderate and Severe Acute Malnutrition as compared to children with normal nutrition
Objectives: Primary: To compare the levels of free carnitine in sera of children with Moderate acute
malnutrition (MAM) and Severe acute malnutrition (SAM) with those with normal nutrition.
Secondary Objectives: 1) To compare proportion of children with carnitine deficiency in children with
MAM & SAM with those with normal nutrition 2) To compare proportion of children with carnitine
insufficiency in children with MAM & SAM with those with normal nutrition 3) To determine the
association between free carnitine levels and lipid profile, total protein and serum albumin in children
with undernutrition 4) To determine the association between free carnitine levels and age, gender,
weight for length/height and mid upper arm circumference in children with undernutrition
Setting: This study will be conducted in the Department of Pediatrics & Department of Biochemistry
of UCMS and GTB Hospital, New Delhi
Collaborating Institution: Department of Genetics & Laboratory, MAMC, New Delhi.
Study design: Comparative Cross-Sectional study
Study duration: 1st August 2025 – 30th November 2026
Sample Size
This is an exploratory study as no previous study has estimated the free carnitine levels in sera of
children with moderate and severe acute malnutrition as per the WHO criteria 2013 [11]. Therefore,
we will be including 30 participants each with moderate and severe acute malnutrition and 30 each
age and sex matched children of normal nutrition with MAM and SAM. Therefore, total sample size
will be 120 children.
PARTICIPANTS:
Inclusion Criteria 1) Cases: All children aged between 6 months to 59 months, visiting pediatric
OPD or admitted in pediatric emergency or pediatric ward will be screened for enrollment. i) Group 1:
Children aged between 6 months-59 months with moderate acute malnutrition (weight for
length/height Z-score between -3 to -2 and/or mid-upper-arm circumference between 11.5 cm-12.5
cm) ii) Group 2: Children aged between 6 months-59 months with severe acute malnutrition (weight
for length/height Z-score <-3 and/or mid-upper-arm circumference <11.5 cm) as per WHO criteria
2013 will be enrolled. 2) Comparison group: Children aged 6 months- 59 months (preferably age and
sex-matched ± 2 month with MAM and SAM) with no undernutrition (weight-for-length Z-score
between -1 to +1, and mid-upper-arm circumference >12.5 cm)
Methods: Baseline assessment of all children will be recorded in a pre-designed case record form.
Anthropometric assessment will be done as per WHO guidelines. Two ml of venous blood sample
will be collected for estimation of lipid profile, serum total protein and serum albumin, 2 ml venous
sample will be collected in plain vial for estimation of serum carnitine levels. Dried blood spot with
heel prick will be collected on filter paper for estimation of acylcarnitine levels.
 Outcome Measures: Primary: Serum free carnitine levels
Secondary: 1) Proportion of children with carnitine deficiency 2) Proportion of children
carnitine insufficiency 3) Correlate with lipid profile, total protein and serum albumin 4) Correlate
with age, gender, weight for height and MUAC
Statistical Analysis: All data will be entered in a Microsoft excel sheet and will be analyzed using
Statistical Package for Social Science (SPSS) statistical software. Descriptive statistics will include
proportion for categorical variables and mean (SD) or median (IQR) or arithmetic/geometric mean
(SD) for carnitine levels. Serum carnitine levels will be compared between the two groups using
ANOVA test. Proportion of children with carnitine deficiency between the two groups will be
compared by Chi square test/Fischer test whichever is applicable. Serum carnitine levels will be
correlated with age, gender, weight for height, MUAC, lipid profile, serum albumin and serum total
protein will be analyzed by Pearson’s/Spearmen Correlation. P<0.05 will be the level of statistical
significance.
 
Close