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CTRI Number  CTRI/2026/01/100014 [Registered on: 01/01/2026] Trial Registered Prospectively
Last Modified On: 02/02/2026
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Dentistry 
Study Design  Randomized, Parallel Group, Multiple Arm Trial 
Public Title of Study   Comparing different tools used for root canal treatment in children aged 4 to 9 years 
Scientific Title of Study   Comparative evaluation of hand files and two rotary systems for pulpectomy in children aged 4-9 years: A Randomised Clinical Trial 
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 Snehal Kumthekar 
Designation   
Affiliation  KAHERs KLE V.K. Institute of Dental Sciences, Belagavi 
Address  KLE Dental College Gate, JNMC Campus, Neharunagar

Belgaum
KARNATAKA
590010
India 
Phone  07385209187  
Fax    
Email  snehalkumthekar1999@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Shivayogi M Hugar 
Designation  Professor 
Affiliation   
Address  KLE Dental College Gate, JNMC Campus, Neharunagar

Belgaum
KARNATAKA
590010
India 
Phone  9986436448  
Fax    
Email  drhugarsm@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Shivayogi M Hugar 
Designation  Professor 
Affiliation   
Address  KLE Dental College Gate, JNMC Campus, Neharunagar

Belgaum
KARNATAKA
590010
India 
Phone  9986436448  
Fax    
Email  drhugarsm@gmail.com  
 
Source of Monetary or Material Support  
Department of Pediatric and Preventive Dentistry, KLE VK Institute of Dental Sciences, Belagavi  
 
Primary Sponsor  
Name  Dr Snehal Sunil Kumthekar 
Address  Department of Pediatric and Preventive Dentistry, KAHERs KLE VK Institute of Dental Sciences, JNMC Campus, Neharu Nagar, Belagavi, 590010, Karnataka, India 
Type of Sponsor  Other [Self] 
 
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 Snehal Kumthekar  KLE VK Institute of Dental Sciences  Department of Pediatric and Preventive Dentistry, Department No. 6, First floor, KAHERs KLE VK Institute of Dental Sciences, JNMC Campus, Nehru Nagar,
Belgaum
KARNATAKA 
07385209187

snehalkumthekar1999@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Research and Ethics Committee KLE VKIDS  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K040||Pulpitis,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Hand Files  To check obturation quality using Hand Files for single sitting Pulpectomy procedures. Treatment will be done in 45 minutes  
Intervention  Kedo Nano Plus Rotary Files  To check obturation quality using Kedo Nano Plus Rotary Files for single sitting Pulpectomy procedures. Treatment will be done in 45 minutes  
Intervention  Neoendo Pedoflex Rotary Files  To check obturation quality using Neoendo Pedoflex Rotary Files for single sitting Pulpectomy procedures. Treatment will be done in 45 minutes 
 
Inclusion Criteria  
Age From  4.00 Year(s)
Age To  9.00 Year(s)
Gender  Both 
Details  • Children in the age group of 4-9 years
• Children with Frankl’s behavior rating scale of definitely positive (++) and positive (+)
• Tooth with the history of spontaneous pain
• Tooth with irreversible pulpitis
• Primary molars with at least remaining two third of the root length
 
 
ExclusionCriteria 
Details  1. Children with systemic diseases and special health care needs
2. Non-vital teeth having signs of abscess, sinus and fistula
3. Primary molars with pathologic mobility and evidence of root
fracture, trauma
4. Primary molars having furcation radiolucency
5. Primary molars with calcified root canals
6. Primary molars with more than two third root resorption, internal
resorption and developmental anomalies
7. Patients who are not willing to undergo treatment 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Obturation Quality
 
Obturation Quality
 
 
Secondary Outcome  
Outcome  TimePoints 
Instrumentation Time
 
From starting of CMP to the last files used 
Postoperative Pain

 
At 24hrs, 48hrs,72hrs 
 
Target Sample Size   Total Sample Size="75"
Sample Size from India="75" 
Final Enrollment numbers achieved (Total)= "75"
Final Enrollment numbers achieved (India)="75" 
Phase of Trial   N/A 
Date of First Enrollment (India)   06/01/2026 
Date of Study Completion (India) 31/01/2026 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Completed 
Recruitment Status of Trial (India)  Completed 
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 Principal Investigator will perform the procedure under Standard Operating Protocols. Patients allocated to Group I will be treated using Hand files, Group II will be treated using Kedo Nano Plus Rotary Files and In Group III Neoendo Pedoflex Files will be used. The teeth selected for the study will be isolated using Rubber dam and the pulpectomy procedure will be carried out in primary molars. The post-operative evaluation of the obturation quality will be done using Modified Coll and Sedrian criteria Instrumentation Time will be recorded using stopwatch. Evaluation of postoperative pain will be done using the Wong-Baker Faces Pain Rating Scale. Parents/guardians will be instructed to record pain on the scale at 24, 48, and 72 h, which will be given to them along with the patient’s information sheet. All the pain scores will be recorded telephonically and the collection of the Patient information sheet will be done on the subsequent follow up visit. Postoperative instructions will be given.


 
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