| 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
|
|
|
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
|
|
|
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
|
|
|
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. |