FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
CTRI Number  CTRI/2025/10/095772 [Registered on: 09/10/2025] Trial Registered Prospectively
Last Modified On: 08/10/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   This study will test if giving prophylactic antibiotics can reduce infections and improve safety for children with acute lymphoblastic leukemia during the early intensive phase of chemotherapy 
Scientific Title of Study   A randomised control trial to determine the efficacy of antibiotic prophylaxis during intensive phase of chemotherapy in children with Acute lymphoblastic leukaemia. 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
IEC-INT/2025/DM-2808 version 1  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Sonali Aggarwal 
Designation  Senior resident 
Affiliation  Post Graduate Institute of Medical Education and Research 
Address  Advanced Pediatric Centre, Post Graduate Institute of Medical Education and Research, Chandigarh

Chandigarh
CHANDIGARH
160009
India 
Phone  8923594612  
Fax    
Email  sonaliaggarwal210@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Amita Trehan 
Designation  Professor 
Affiliation  Post Graduate Institute of Medical Education and Research, Chandigarh 
Address  Advanced Pediatric Centre, Post Graduate Institute of Medical Education and Research, Chandigarh

Chandigarh
CHANDIGARH
160009
India 
Phone  9815228866  
Fax    
Email  trehanamita@hotmail.com  
 
Details of Contact Person
Public Query
 
Name  Sonali Aggarwal 
Designation  Senior resident 
Affiliation  Post Graduate Institute of Medical Education and Research, Chandigarh 
Address  Advanced Pediatric Centre, Post Graduate Institute of Medical Education and Research, Chandigarh

Chandigarh
CHANDIGARH
160009
India 
Phone  8923594612  
Fax    
Email  sonaliaggarwal210@gmail.com  
 
Source of Monetary or Material Support  
Nil 
 
Primary Sponsor  
Name  Sonali Aggarwal 
Address  Advanced Pediatric Centre, Post Graduate Institute of Medical Education and Research 
Type of Sponsor  Other [Self] 
 
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 
Sonali Aggarwal  Post Graduate Institute of Medical Education and Research  Advanced Pediatric Centre, Post Graduate Institute of Medical Education and Research
Chandigarh
CHANDIGARH 
8923594612

sonaliaggarwal210@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Post Graduate Institute of Medical Education and Research, Chandigarh Institutional Ethics Committee (Intramural)  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: C910||Acute lymphoblastic leukemia [ALL],  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Antibiotic prophylaxis  Oral Levofloxacin 
Comparator Agent  Standard practice  Standard practice 
 
Inclusion Criteria  
Age From  1.00 Year(s)
Age To  12.00 Year(s)
Gender  Both 
Details  Diagnosed cases of Acute lymphoblastic leukaemia (high risk/ intermediate risk) during induction of remission and consolidation phase of therapy. 
 
ExclusionCriteria 
Details  Relapsed acute lymphoblastic leukemia, infant leukaemia, refusal to consent, infective focus or bacteria at the time of diagnosis, allergy to quinolones. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Primary outcomes
1. Incidence of febrile neutropenia in both the groups.
2. Incidence of bacteria/microbiologically documented infections (MDI) in both the groups.
 

From start of Induction of remission to end of consolidation therapy
 
 
Secondary Outcome  
Outcome  TimePoints 
Secondary outcomes
A. Assessment of the severity of febrile neutropenia between the groups.
1. Need for hospital admission
2. Need for Pediatric Intensive care unit admission.
3. Incidence of clinical complications.
4. Duration of hospitalization.
5. Mortality
B. Risk associated with antibiotic prophylaxis.
1. Incidence of multi drug resistant organisms.
2. Incidence of invasive fungal infections.
3. Incidence of Clostridium difficle diarrhoea. 
From start of Induction of remission to end of consolidation therapy 
 
Target Sample Size   Total Sample Size="118"
Sample Size from India="118" 
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)   20/10/2025 
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="0"
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  

The treatment of acute lymphoblastic leukemia (ALL) has evolved significantly in the recent years. The overall and 5-year survival rates for children with ALL approach  90 percent. This is due to better understanding of genetics and  biological features of leukemic cells, resulting in  better risk stratification of children and optimization of treatment regimens through national and international collaboration.

 

However, despite these high cure rates, the main problem is the treatment related mortality (TRM), which is estimated to be 4% in the developed countries . TRM is much higher in Low middle income countries (LMIC’s), ranging from 11 to 25 percent. Among these deaths, the most frequent causes are febrile neutropenia and infections mainly bacterial, which occur more frequently during intensive chemotherapy phase, such as induction. These infections not only directly lead to deaths, but can also cause delay in chemotherapy treatment, which can, in turn, lead to increase in relapses.

 

Treatment related mortality contributes to a decrease in survival in LMIC’s . Infection rates are high in LMIC’s attributable to a large number of factors which include poor hygiene, overcrowding , undernutrition , poor access to urgent care and environmental factors such as poor sanitation , heat and humidity. Therefore, to reduce the risks related to infections in these patients, use of systemic antimicrobial prophylaxis can be possible approach.

 

There is literature that shows the use of antibiotic prophylaxis in adult patients during intensive chemotherapy to reduce bacteremia and improve outcomes. In 2016, National Comprehensive Cancer network (NCCN) had recommended fluroquinolones (FQs) prophylaxis for adult patients with hematological malignancies.

 

The use of antibiotic prophylaxis is still controversial in pediatric patients due to lack of data on effectiveness and best choice of antibiotic. However, there are few studies that have shown that prophylactic use of levofloxacin in patients with hematological malignancies has resulted in significant decrease in bacteremia. But the use of antibiotic prophylaxis is also associated with an increase in risk of FQs - resistant Gram negative bacteria development, invasive fungal infections (IFD), Clostridioides difficle (C.diffcile) infections and musculoskeletal toxicities. Thus, both the 8th European Conference on Infections in Leukemia (ECIL-8) and the Children’s Oncology Group do not currently support routine antibiotic prophylaxis in pediatric patients with acute leukemia.

More randomized prospective studies are required in pediatric patients to demonstrate the benefits of using antibiotic prophylaxis and to monitor for the emergence of resistant bacterias, C.difficle infections and IFD. With this background, this study aims to assess the efficacy and risk of levofloxacin prophylaxis in children with ALL receiving intensive chemotherapy.

 

 
Close