FULL DETAILS (Read-only)  -> Click Here to Create PDF for Current Dataset of Trial
CTRI Number  CTRI/2025/07/091780 [Registered on: 25/07/2025] Trial Registered Prospectively
Last Modified On: 25/07/2025
Post Graduate Thesis  Yes 
Type of Trial  Observational 
Type of Study   Follow Up Study 
Study Design  Single Arm Study 
Public Title of Study   effectiveness Of acls training  
Scientific Title of Study   retension of acls knowledge after 6 Months Of acls training and effectiveness of refresher video 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  DR PARVAT KADIAN 
Designation  EMERGENCY RESIDENT 
Affiliation  BLK HOSPITAL 
Address  EMERGENCY WARD IN EMERGENCY DEPARTEMENT BLK MAX SUPER SPECIALTY HOSPITAL RAJENDER NAGAR NEW DELHI

Central
DELHI
110005
India 
Phone  9466888005  
Fax    
Email  parvatkadian@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Saloni Paranjape 
Designation  Senior consultant 
Affiliation  Blk Hospital 
Address  second floor Ot complex departement of anesthesia blk Rajendra Nagar new delhi

Central
DELHI
110005
India 
Phone  9466888005  
Fax    
Email  drsaloni@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Saloni Paranjape 
Designation  Senior Consultant 
Affiliation  Blk hospital 
Address  second floor Ot complex department of anesthesia blk max rajendra nagar new delhi

Central
DELHI
110005
India 
Phone  9466888005  
Fax    
Email  drsaloni@gmail.com  
 
Source of Monetary or Material Support  
all nursing staff 
 
Primary Sponsor  
Name  dr parvat kadian 
Address  emergency ward in emergency departement blk hospital rajendra nagar new delhi 
Type of Sponsor  Private hospital/clinic 
 
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 
dr saloni  blk max Hospital   second floor Ot complex blk max hospital pusa road rajendra nagar new delhi
Central
DELHI 
9466888005

drsaloni@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
INSTITUTIONAL ETHICS COMMITTEE  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  RETENSION ACLS KNOWLEDGE 
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  nil  obeservation study 
Intervention  Nil  observational 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  healthcare professional 
 
ExclusionCriteria 
Details  1. All Previous ACLS Certification .
2.Pregnant Women. 
 
Method of Generating Random Sequence    
Method of Concealment    
Blinding/Masking    
Primary Outcome  
Outcome  TimePoints 
TO EVALUATE THE EXTENT OF KNOWLEDGE RETENSION OF ACLS TRAINING  24 weeks 
 
Secondary Outcome  
Outcome  TimePoints 
to evaluate the knowledge of healthcare professional in acls training  24 weeks 
 
Target Sample Size   Total Sample Size="50"
Sample Size from India="50" 
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)   05/08/2025 
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="1"
Months="5"
Days="5" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
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   Retension of acls knowledge after 24 weeks of training and evaluation of video based training effectiveness after 6 months 
Close