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CTRI Number  CTRI/2024/05/067939 [Registered on: 27/05/2024] Trial Registered Prospectively
Last Modified On: 02/03/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Diagnostic 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Effect of dietary changes on normal FDG uptake in the bowel. 
Scientific Title of Study   Effect of dietary modification on physiological 18F FDG uptake in the bowel. 
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 Vaibhav Jain 
Designation  Resident, Nuclear Medicine 
Affiliation  Army Hospital Research and Referral  
Address  Department of Nuclear Medicine Army Hospital Research and Referral Delhi Cantt
Delhi Cantt
South West
DELHI
110010
India 
Phone  9823980753  
Fax    
Email  vaibhav_0916@yahoo.com  
 
Details of Contact Person
Scientific Query
 
Name  Brig Dr AVS Anil Kumar 
Designation  Consultant Medicine and Nuclear Medicine 
Affiliation  Army Hospital Research and Referral  
Address  Department of Nuclear Medicine Army Hospital Research and Referral Delhi Cantt
Delhi Cantt
South West
DELHI
110010
India 
Phone  9673117027  
Fax    
Email  nmdahrr@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Vaibhav Jain 
Designation  Resident, Nuclear Medicine 
Affiliation  Army Hospital Research and Referral  
Address  Department of Nuclear Medicine Army Hospital Research and Referral Delhi Cantt
Delhi Cantt
South West
DELHI
110010
India 
Phone  9823980753  
Fax    
Email  vaibhav_0916@yahoo.com  
 
Source of Monetary or Material Support  
Department of Nuclear Medicine Army Hospital Research and Referral Delhi Cantt New Delhi- 110010 
 
Primary Sponsor  
Name  Dr Vaibhav Jain 
Address  Department of Nuclear Medicine Army Hospital Research and Referral Delhi Cantt New Delhi- 110010 
Type of Sponsor  Other [Thesis- self initiated] 
 
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 Vaibhav Jain  Army Hospital Research and Referral   Department of Nuclear Medicine Army Hospital Research and Referral Delhi Cantt
South
DELHI 
9823980753

vaibhav_0916@yahoo.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee Army Hospital (R&R), Delhi Cantt  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: D499||Neoplasm of unspecified behavior of unspecified site,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Dietary modification in patients undergoing PET/CT scan.  Low carbohydrate and high fat diet in patients undergoing FDG PET/CT scan 48 hours priors to the scan. 
Comparator Agent  Routine diet in patients undergoing PET/CT scan.  Routine diet for 48 hours prior to FDG PET/CT scan. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  70.00 Year(s)
Gender  Both 
Details  Patients undergoing PET/CT scan 
 
ExclusionCriteria 
Details  Diabetics
On drugs affecting gut motility
Known bowel disease
poor general condition
pregnant and lactating women 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To determine whether a statistically significant reduction in FDG uptake in bowel with LCHF diet compared to a standard diet  Baseline 
 
Secondary Outcome  
Outcome  TimePoints 
To evaluate the effect of diet on intestinal 18F- FDG uptake by measuring SUV max of different parts of intestine.   scan done 60 minutes after FDG injection 
 
Target Sample Size   Total Sample Size="200"
Sample Size from India="200" 
Final Enrollment numbers achieved (Total)= "125"
Final Enrollment numbers achieved (India)="125" 
Phase of Trial   Phase 3/ Phase 4 
Date of First Enrollment (India)   01/07/2024 
Date of Study Completion (India) Date Missing 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) 02/09/2025 
Estimated Duration of Trial   Years="1"
Months="9"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details
Modification(s)  
N/A 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary  

AIMS AND OBJECTIVES

 


Aim: To evaluate the effect of dietary modification with low carbohydrate, high fat (LCHF) diet on intestinal 18F-FDG uptake.


 Objectives: The present study intends to:

1. To compare SUV max value of physiological FDG uptake in routine diet and LCHF diet.

 

2.  To evaluate the effect of diet on intestinal 18F- FDG uptake by measuring SUV max of different parts of intestine.

Site: Department of Nuclear Medicine, Army Hospital Research and Referral, New Delhi.

 

Block Randomization

The research will employ a Block Randomization strategy using the Sealed Envelope System. Ten sealed opaque envelopes, labelled A and B (5 envelopes each) will be prepared. Among these, 5 envelopes will be assigned to the Native group (Routine Diet), and 5 to the LCHFD group. Upon a patient’s consent to participate, an envelope will be randomly chosen and opened, determining the group allocation for the patient. This randomization approach will involve 20 blocks, each comprising 10 patients. In each block, 5 patients will be designated to the Native group, and the remaining 5 to the LCHFD group.

Inclusion criteria: 

Patients undergoing PET/CT scan. 

Exclusion criteria: 

l   Unwilling patients

l   Known diabetics.

l   Drugs affecting gut motility and uptake.

l   Serum glucose level of more than 200 mg/dl

l   Failure to fast

l   Failure to comply with dietary modification.  

l   Known bowel disease.

l   Patients with sepsis

l   Patients with deranged hematology and biochemistry parameters.

l   Pregnant and lactating women.

l   Patients unable to undergo PET/CT

l   Claustrophobic patients.

  

Data collection:

·         All patients will be subjected to a thorough clinical evaluation as per standard guideline.

·         Patient’s details including history, clinical examination findings, relevant investigation & treatment history will be recorded as per proforma attached.

 

 

Methods:

l   Patients will be randomly assigned into 2 groups, with one group taking a routine diet (RD) and the other an LCHFD for 48 h before the 18F-FDG PET/CT scan. All patients will receive the required details about their diet and will be instructed to fast for at least 6 h before the study.

VEGETARIAN

l   BUTTER- 100GM

l   PANEER/CHEESE

l   ROTI- ONLY 1 OR BREAD- ONLY 2 SLICES OR RICE- 1 BOWL

l   SOYA

l   CURD

l   NUTS

l   SELECTED FRESH VEGETABLES

NON-VEGETARIAN

l   EGGS

l   FRIED/ ROASTED CHICKEN

l   FRIED/ROASTED MUTTON

l   FRIED/ROASTED FISH

l   For 48 h before the study any carbohydrate-containing beverages or meals will be avoided.

 

l   Computer generated randomization (block randomization) will be done.

 

l   Allocation concealment will be done using opaque envelope.

 

l   PET/CT will be performed approximately 60 min after intravenous administration of 392 + 63 MBq (10.6 + 1.7 mCi) of 18F-FDG according to body weight (5.2 MBq/kg [0.14 mCi/kg]) using a whole-body four-ring dedicated LYSO PET/ CT scanner - GE Discovery MI DR. CT images will be obtained using 120 KV and auto mAs for CT based attenuation correction and localization of the lesions. Images will be reconstructed using standard iterative algorithm (OSEM) and reformatted into Transaxial, Coronal and Sagittal views. A 3D image and fusion images of PET & CT will be obtained.

 

·         18F-FDG PET/CT scan findings will be interpreted independently by 2 nuclear medicine physicians. Patients with high tumour volume load or inadequate myocardial suppression will be excluded from the study.

 

l   The uptake in the small intestine and different parts of the large bowel (Duodenum, Jejunum, Ileum, ICJ, Ascending colon, Descending colon, Transverse colon, Hepatic flexure, Splenic flexure, Sigmoid Colon and Rectum) will be assessed quantitatively using SUVmax and qualitatively using visual assessment score.

 

l   The intensity of uptake in the different parts of intestine will be classified qualitatively based on visual assessment. The visual assessment score is based on the Likert scale used for Myocardial FDG uptake.

 

SCORE

PATTERN

0

No uptake/ homogeneously minimal uptake

1

Heterogeneous Mild Uptake

2

Moderate or Mostly Intense uptake

3

Homogeneously Intense uptake

 
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