FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
CTRI Number  CTRI/2026/02/103436 [Registered on: 09/02/2026] Trial Registered Prospectively
Last Modified On: 09/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Observational 
Type of Study   A Prospective Observation Study 
Study Design  Other 
Public Title of Study   Effect of drug colistin in newborn infection. 
Scientific Title of Study   To study the efficacy and outcome of intravenous colistin therapy in culture positive multidrug resistant or extensively drug resistant sepsis in outborn neonates.A prospective observation study 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Mamta Jajoo 
Designation  Professor Pediatrics 
Affiliation  Chacha Nehru Bal Chikitsalaya 
Address  Department of Pediatrics Chacha Nehru Bal Chikitsalaya Geeta colony Delhi
Geeta Colony Delhi 110031
East
DELHI
110031
India 
Phone  8595919301  
Fax    
Email  mamtajajoo123@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Goutham Shivarag 
Designation  MD Pediatrics Junior Resident 
Affiliation  Chacha Nehru Bal Chikitsalaya 
Address  Chacha Nehru Bal Chikitsalaya Geeta Colony Delhi
Geeta Colony Delhi 110031
East
DELHI
110031
India 
Phone  7907593387  
Fax    
Email  goutham007vv@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Goutham Shivarag 
Designation  MD Pediatrics Junior Resident 
Affiliation  Chacha Nehru Bal Chikitsalaya 
Address  Chacha Nehru Bal Chikitsalaya Geeta Colony Delhi
Geeta Colony Delhi 110031
East
DELHI
110031
India 
Phone  7907593387  
Fax    
Email  goutham007vv@gmail.com  
 
Source of Monetary or Material Support  
Chacha Nehru Bal Chikitsalaya Geeta Colony Delhi 110031 
 
Primary Sponsor  
Name  Chacha Nehru Bal Chikitsalaya 
Address  Geeta Colony Delhi 110031 
Type of Sponsor  Other [Autonomous Institute under Goverment of NCT of Delhi] 
 
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 
Office  Dept of neonatology ,Dept of pediatrics medicine,2nd floor ICU block,Chacha Nehru Bal Chikitsalaya  PUSHTA ROAD ,Geeta Colony Delhi 110031
East
DELHI 
8595919370

cnbc2003@yahoo.co.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
The Institutional Ethics Committee,Chacha Nehru Bal Chikitsalaya, Geeta Colony,Delhi,110031  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: B96||Other bacterial agents as the cause of diseases classified elsewhere, (2) ICD-10 Condition: B961||Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified elsewhere, (3) ICD-10 Condition: B962||Escherichia coli [E. coli ] as thecause of diseases classified elsewhere, (4) ICD-10 Condition: B965||Pseudomonas (aeruginosa) (mallei)(pseudomallei) as the cause of diseases classified elsewhere, (5) ICD-10 Condition: B968||Other specified bacterial agents as the cause of diseases classified elsewhere,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Nil  Nil 
 
Inclusion Criteria  
Age From  0.00 Day(s)
Age To  28.00 Day(s)
Gender  Both 
Details  All neonates with confirmed positive culture of any sterile body fluid like blood, respiratory ,urinary tract caused by multidrug or extensively drug resistant gram negative bacteria and susceptibility confirmed to colistin 
 
ExclusionCriteria 
Details  Children with major congenital anomalies, severe renal dysfunction at baseline . Cases with colistin administered less than 48 hours. Cases with CSF culture emerged multidrug or extensively drug resistant organisms 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Clinical cure at day 14 (defined as resolution of symptoms or signs of infection without need of antibiotic change or escalation.  Clinical cure at day 14 (defined as resolution of symptoms or signs of infection without need of antibiotic change or escalation. 
 
Secondary Outcome  
Outcome  TimePoints 
Microbiological Eradication as repeat culture report negative for Multidrug or Extensively drug resistant organisms.  72 hour , day 7 , day 14 
All cause mortalities.  48 hours to 14 days or till Discharge. 
Neonates developing Acute Kidney Injury as per N KDIGO  24 hour , 72 hour , day 7 
Neonates developing hypocalcemia ,hypomagnesemia & dyselectrolytemia.  24 hour ,72 hour , day 7 
Neonates requiring additional antibiotics in monotherapy group.  starting of therapy to end of therapy 
 
Target Sample Size   Total Sample Size="80"
Sample Size from India="80" 
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)   20/02/2026 
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="0"
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  

SUMMARY

Sepsis is a systemic inflammatory response syndrome caused by infection and accompanied by pathological inflammation and organ system dysfunction. Neonatal sepsis continues to be a significant contributor to neonatal morbidity and mortality globally, particularly in low- and middle-income countries (LMICs) such as India The burden is even more pronounced in outborn neonates.

In India over two-thirds of isolates were gram-negative organisms. These organisms are now frequently multidrug-resistant (MDR) or extensively drug-resistant (XDR). The rise of MDR and extensively drug-resistant (XDR) strains has posed a formidable challenge to clinicians as infections caused by these pathogens are resistant to all commonly used antibiotics, leaving limited treatment options. In India, weak enforcement of regulations surrounding over-the-counter antibiotic sales, their affordability, and a surge in usage driven by economic growth and prosperity significantly contribute to the rise of antibiotics resistance The situation has led to the reconsideration of older antibiotics, including the polymyxins—primarily colistin (polymyxin E)—as agents of last resort.

In India, neonatal units, particularly in tertiary care referral hospitals have adopted colistin into their sepsis treatment algorithms. There is a lack of standardized clinical guidelines for administering intravenous colistin to neonates. Most existing recommendations are derived from adult studies, limited pediatrics research, and a few retrospective investigations involving neonates. Although colistin has shown efficacy in treating multidrug-resistant (MDR) Gram-negative bacterial infections in this population, the variability in treatment outcomes indicates the need for further research. Several factors can affect treatment success, including the timing of therapy initiation, dosage, in vivo bacterial susceptibility, concurrent use of other antibiotics with colistin, severity of sepsis, and the presence of comorbidities. To establish clearer efficacy and safety benchmarks and identify predictors of positive outcomes, prospective studies are essential. This study aims to provide evidence regarding the clinical outcomes, survival rates, and microbiological responses of colistin in outborn neonates (infants born outside a tertiary perinatal unit) centers. Proportion of neonates showing microbiological clearance with IV colistin therapy. This study is also directed to study about, Proportion of neonates having adverse effects like Acute Kidney Injury, electrolyte disturbances like hypokalaemia, hypomagnesemia. To compare the effect of colistin monotherapy versus colistin multidrug therapy showing. on microbiological cure. To compare the mortality and clinical outcomes of colistin monotherapy versus colistin multidrug therapy, To study the duration of Colistin therapy and its correlation with duration of hospital stay.

 
Close