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CTRI Number  CTRI/2025/07/090305 [Registered on: 07/07/2025] Trial Registered Prospectively
Last Modified On: 04/07/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Dentin remineralization using Vitamin D3 versus Calcium hydroxide as indirect pulp capping agents 
Scientific Title of Study   Clinical and radiographic assessment of dentin remineralization using Vitamin D3 versus Calcium hydroxide as indirect pulp capping agents in primary molars – Randomized 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 V Aparna 
Designation  Post Graduate 
Affiliation  Vinayaka Missions Sankarachariyar Dental College 
Address  Room no - 6, Department of Pediatric Dentistry, Vinayaka Missions Sankarachariyar Dental College NH-47 Sankari main road Ariyanoor Salem - 636308

Salem
TAMIL NADU
636308
India 
Phone  9894810759  
Fax    
Email  aparnavvarthan@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Veena Arali 
Designation  HOD 
Affiliation  Vinayaka Missions Sankarachariyar Dental College 
Address  Room no - 6, Department of Pediatric Dentistry, Vinayaka Missions Sankarachariyar Dental College NH-47 Sankari main road Ariyanoor Salem - 636308

Salem
TAMIL NADU
636308
India 
Phone  8355803238  
Fax    
Email  empendurkar@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr V Aparna 
Designation  Post Graduate 
Affiliation  Vinayaka Missions Sankarachariyar Dental College 
Address  Room no - 6, Department of Pediatric Dentistry, Vinayaka Missions Sankarachariyar Dental College NH-47 Sankari main road Ariyanoor Salem - 636308

Salem
TAMIL NADU
636308
India 
Phone  9894810759  
Fax    
Email  aparnavvarthan@gmail.com  
 
Source of Monetary or Material Support  
Room no - 6, Department of Pediatric Dentistry, Vinayaka Missions Sankarachariyar Dental College, NH-47 Sankari main road Ariyanoor Salem - 636308  
 
Primary Sponsor  
Name  Dr V Aparna 
Address  Vinayaka Missions Sankarachariyar Dental College NH-47 Sankari main road Ariyanoor Salem - 636308 
Type of Sponsor  Other [Dental] 
 
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 V Aparna  Vinayaka Missions Sankarachariyar Dental College   Room no - 6, Department of Pediatric Dentistry, NH-47 Sankari main road Ariyanoor Salem - 636308
Salem
TAMIL NADU 
9894810759

aparnavvarthan@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Committee of VMS Dental College  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Dental treatment 
Patients  (1) ICD-10 Condition: K040||Pulpitis,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Calcium hydroxide powder  0.25g of Calcium hydroxide powder mixed 2 drops of saline and used as an indirect pulp capping material once 
Intervention  Vitamin D powder  0.25g of Vitamin D powder mixed with 2 drops of saline and used as an indirect pulp capping material once 
 
Inclusion Criteria  
Age From  5.00 Year(s)
Age To  10.00 Year(s)
Gender  Both 
Details  No history of spontaneous and nocturnal pain
No history of swelling or sinus tracts
No radiographic signs of pathologic root resorption and furcation radiolucency
Dental caries involving more than 2/3rd of the dentin thickness not approaching pulp
 
 
ExclusionCriteria 
Details  Signs of irreversible pulpitis
Patients who are unwilling to participate in the study
Patients with systemic diseases/ physical disabilities
 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Investigator Blinded 
Primary Outcome  
Outcome  TimePoints 
Identify the most effective indirect pulp capping material  Baseline, 2 months, 6 months 
 
Secondary Outcome  
Outcome  TimePoints 
Nil  Nil 
 
Target Sample Size   Total Sample Size="60"
Sample Size from India="60" 
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)   15/07/2025 
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="0"
Months="6"
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  

Dental caries continues to be a major health concern and is also the most common dental disease, with increased prevalence among young children. Dental caries in proximity to pulp are commonly treated with a vital pulp procedure rather than a restorative technique to preserve the vitality of the primary tooth. Indirect pulp capping is where the deepest layer of the remaining affected carious dentin is covered with a layer of biocompatible material to prevent pulpal exposure and further trauma to the pulp. Vitamin D3 plays a crucial role in regulating bone metabolism and mineralization of skeletal and dental tissues. Calcium hydroxide is a material with a long history of clinical success, considered the gold standard among other pulp capping agents. It has an antibacterial activity, and it stimulates the remineralization of the remaining carious dentin. Literature review revealed an in vitro study in which Vitamin D3 is being used for odontogenic differentiation. The current study is designed to compare the efficacy of Vitamin D3 and Calcium hydroxide as indirect pulp capping agents in primary teeth at baseline, 2nd, and 6th month follow-up.

HYPOTHESIS: There is no difference between the efficacy of Vitamin D3 and Calcium hydroxide when used as indirect pulp capping agents.

METHOD:

Study design: Randomized Clinical Trial

Sample size: 60 Children (30/Group).  Source of study: Department of Paediatric and Preventive Dentistry, VMSDC, Salem. 

Inclusion Criteria:

  • No history of spontaneous and nocturnal pain
  • No history of swelling or sinus tracts
  • No radiographic signs of pathologic root resorption and furcation radiolucency
  • Dental caries involving more than 2/3rd of the dentin thickness, not approaching the pulp

Exclusion criteria:

  • Signs of irreversible pulpitis
  • Patients who are unwilling to participate in the study
  • Patients with systemic diseases/ physical disabilities

Randomization:

The randomization is achieved by a simple randomization technique using the lottery method.

Based on the inclusion criteria, a total of 60 children in the age group of 5-10 years will be selected for the study. Study participants will be allocated into 2 groups. Following Rubber dam placement, soft caries (infected dentin) removal will be done using a slow-speed handpiece and a carbide bur.

Group I - Vitamin D3 (Powder)

Vitamin D3 powder will be mixed with saline and delivered using a spoon excavator to the base of the cavity and condensed using a sterile cotton pellet moistened with saline.

Group II - Calcium Hydroxide (Powder)

Calcium hydroxide powder will be mixed with saline and delivered using a spoon excavator to the base of the cavity and condensed using a sterile cotton pellet moistened with saline.

 A thick mix of type IX restorative Glass Ionomer Cement (GIC) will be placed over the indirect pulp capping agents and restored. Postoperative IOPA with Grid and film holder will be taken in paralleling technique to check the remaining dentin thickness (RDT), which will serve as the Baseline parameter. Periodic clinical and radiographic evaluations will be carried out at the 2nd and 6th months post-operatively.

Clinical Assessment:

The evaluations will be performed at baseline and at 2nd and 6th month intervals through a clinical examination according to Zurn and Seale’s pain rating scale, 2008.

Radiographic Assessment:

The evaluations will be performed at baseline and 2nd and 6th month intervals through a radiological examination. Radiographic success will be confirmed by the absence of any pathological root resorption, furcal radiolucency. IOPA grids, which are made up of copper wire, will be used with film holders. The paralleling technique will be used. The IOPA grids, when superimposed with film, show anatomic structures with grid lines. These grid lines are evenly distributed, which is 1mm part lengthwise and widthwise. The dentin remineralisation is evaluated by using a digital radiographic technique superimposed with radiolucent grid lines.

 
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