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CTRI Number  CTRI/2014/09/005050 [Registered on: 24/09/2014] Trial Registered Retrospectively
Last Modified On: 28/12/2018
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Process of Care Changes 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study
Modification(s)  
Fluid bolus administration over 15-20 minutes versus 5-10 minutes each in children with septic shock 
Scientific Title of Study   Administration of fluid bolus over 15-20 minutes versus 5-10 minutes in children with septic shock in the ‘first hour’ of resuscitation– A Randomized Controlled Trial 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Jhuma Sankar 
Designation  Associate Professor 
Affiliation  PGIMER, Dr RML Hospital 
Address  Room-403, Department of Pediatrics, PGIMER, Dr RML Hospital

Central
DELHI
110001
India 
Phone    
Fax    
Email  jhumaji@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Jhuma Sankar 
Designation  Associate Professor 
Affiliation  PGIMER, Dr RML Hospital 
Address  Room-403, Department of Pediatrics, PGIMER, Dr RML Hospital

Central
DELHI
110001
India 
Phone    
Fax    
Email  jhumaji@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Jhuma Sankar 
Designation  Associate Professor 
Affiliation  PGIMER, Dr RML Hospital 
Address  Room-403, Department of Pediatrics, PGIMER, Dr RML Hospital

Central
DELHI
110001
India 
Phone    
Fax    
Email  jhumaji@gmail.com  
 
Source of Monetary or Material Support  
None 
 
Primary Sponsor  
Name  PGIMER Dr RML Hospital 
Address  Baba Kharak Singh Marg; New Delhi 
Type of Sponsor  Research institution and hospital 
 
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 
Jhuma Sankar  PGIMER, Dr RML Hospital  Room no-403 Administrative Block PGIMER, Dr RML Hospital, Baba Kharak Singh Marg, New Delhi
Central
DELHI 
9818399864

jhumaji@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee, PGIMER Dr RML Hospital  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied
Modification(s)  
Health Type  Condition 
Patients  Children 17 years of age with septic shock , (1) ICD-10 Condition: A419||Sepsis, unspecified organism,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Fluid bolus over 15-20 minutes  Fluid bolus of 20 ml/kg would be administered over 15-20 minutes 
Comparator Agent  Fluid bolus over 5-10 minutes  Fluid bolus of 20 ml/kg would be administered over 5-10 minutes 
 
Inclusion Criteria  
Age From  2.00 Month(s)
Age To  17.00 Year(s)
Gender  Both 
Details  Children < 18 years of age with features of septic shock with or without hypotension would be included 
 
ExclusionCriteria 
Details  1. Moderate to severely malnourished children (Indian Academy of Pediatrics classification for malnutrition grades 3 and 4)
2. Primary cardiac illness
3. Contraindication to central venous catheter insertion
4. Children with features of fluid overload at presentation
5. Children whose parents refuse to give an informed consent
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Outcome Assessor Blinded 
Primary Outcome
Modification(s)  
Outcome  TimePoints 
The proportion of children requiring mechanical ventilation and/or impaired oxygenation (Oxygenation Index) in those already on ventilator
 
At 6 and 24 hours of admission 
 
Secondary Outcome  
Outcome  TimePoints 
To assess the effect of intervention on
1.The amount of fluid required (in ml/kg)
2. Inotropic score
3.Proportion of children attaining therapeutic end points
4.Duration of ventilation (in hours)
5.Duration of inotropic support (in hours)
6.Time to achieving therapeutic end points
7.Duration of intensive care unit (ICU) stay
8.Mortality and
9. Serum pro-BNP levels
 
1. Amount of fluid required in first 6 and 24 hours.
2. Inotropic score at 6 and 24 hours.
3. Attaining therapeutic end points at 6 hours.
4. Total duration of ventilation.
5. Total time period to achieving therapeutic end points.
6. Total duration of ICU stay
7. Serum pro BNP levels at 1 and 6 hrs post initial fluid boluses  
 
Target Sample Size   Total Sample Size="220"
Sample Size from India="220" 
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   Phase 4 
Date of First Enrollment (India)
Modification(s)  
16/09/2013 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  16/09/2013 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="2"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Other (Terminated) 
Recruitment Status of Trial (India)  Other (Terminated) 
Publication Details   None 
Individual Participant Data (IPD) Sharing Statement

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

Brief Summary
Modification(s)  

Septic shock in children is most commonly associated with severe hypovolemia. Studies on pediatric septic shock have shown that early and aggressive resuscitation including administration of fluid volumes up to 60ml/kg in the first hour of resuscitation results in 9 fold reduction in mortality in these children. Therefore the management guidelines for septic shock in children advocates aggressive fluid resuscitation of up to 60 ml/kg as boluses of 20ml/kg each over a total duration of 20-30 minutes to achieve desired heart rates, and blood pressure. Although advocated, this duration of administration may not be practical in all types of setups for 2 important reasons a) due to logistics of administering such large volumes in 5-10 minutes (thin veins) and b) due to the fear of fluid overload as most of these facilities may not be equipped to ventilate these children in case fluid overload develops. Not surprisingly therefore, the average time duration reported in pediatric literature till date of administering each bolus has ranged from anywhere between 15-30 minutes per bolus to 45-60 minutes per bolus. Given this background, we decided to compare these two time durations- that is the one proposed (5-10minutes) versus the one commonly used (15-20 minutes) of individual bolus administration on immediate effects such as proportion developing fluid overload and/or proportion requiring mechanical ventilation and critical outcomes such as mortality. There is a plan to enroll 220 subjects over a period of 2 years. The bolus will be administered by manual push in the 5-10 minutes group and by infusion pump timed for 15 minutes in the 15 minute group soon after enrollment. This study will provide an answer to the duration of administration of each fluid bolus in children with septic shock in the first hour of resuscitation. If proven to be superior or similar in terms of primary outcomes the 15-20 minutes time duration may be recommended instead of the 5-10 minutes duration for administration of each fluid bolus thereby ensuring better compliance with the guidelines and improved outcomes in children with septic shock.

 In August 2014, we performed interim analysis after enrolling ~ 50% of patients (n=96) and found that fewer children receiving fluid boluses over 15-20 minutes required mechanical ventilation than those receiving boluses over 5-10 minutes. Due to safety concerns in the group receiving boluses over 5-10 minutes we had to stop the study as per the mandate of the IEC. 

 
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