| 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
|
|
|
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
|
|
|
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. |