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CTRI Number  CTRI/2026/03/106118 [Registered on: 13/03/2026] Trial Registered Prospectively
Last Modified On: 13/03/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia
Screening
Dentistry 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Checking effects of crown implant ratio on crestal bone levels and bone density. 
Scientific Title of Study   Comparative Evaluation Of Different Crown Implant Ratios On Crestal Bone Levels And Bone Density Around The Dental Implant A Clinico Radiographic 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  Dr Abhinit Srivatsav 
Designation  Post Graduate Student 
Affiliation  Coorg institute Of Dental Sciences 
Address  Department of Periodontics Room Number 4 Coorg Institute Of Dental Sciences SH 88B Kodagu Virajpet Aimangala Karnataka
Coorg Institute Of Dental Sciences, SH 88B, Kodagu , Virajpet, Aimangala, Karnataka 571218
Kodagu
KARNATAKA
571218
India 
Phone  09535225866  
Fax    
Email  drabhinitsrivatsav@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Abhinit Srivatsav 
Designation  Post Graduate Student 
Affiliation  Coorg institute Of Dental Sciences 
Address  Department of Periodontics Room Number 4 Coorg Institute Of Dental Sciences SH 88B Kodagu Virajpet Aimangala Karnataka
Coorg Institute Of Dental Sciences, SH 88B, Kodagu , Virajpet, Aimangala, Karnataka 571218
Kodagu
KARNATAKA
571218
India 
Phone  09535225866  
Fax    
Email  drabhinitsrivatsav@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Radhika B 
Designation  Professor 
Affiliation  Coorg institute Of Dental Sciences 
Address  Department of Periodontics Room Number 4 Coorg Institute Of Dental Sciences SH 88B Kodagu Virajpet Aimangala Karnataka
Department of Periodontics Room Number 4 Coorg Institute Of Dental Sciences SH 88B Kodagu Virajpet Aimangala Karnataka
Kodagu
KARNATAKA
571218
India 
Phone  8618772703  
Fax    
Email  radhika_b24@yahoo.co.in  
 
Source of Monetary or Material Support  
Coorg Institute Of Dental Sciences, Dept Of Periodontics And Implantology, Room no. 4 K.K. Campus, Magulla village, Virajpet, Kodagu, Karnataka, 571218 
 
Primary Sponsor  
Name  Dr.Abhinit Srivatsav 
Address  Coorg Institute Of Dental Sciences, Dept Of Periodontics And Implantology, Room no. 4 K.K. Campus, Magulla village, Virajpet, Kodagu, Karnataka, 571218 
Type of Sponsor  Other [Self] 
 
Details of Secondary Sponsor  
Name  Address 
Indian Society of Periodontics  721, Phase 3B-1, Mohali SAS Nagar. 160060 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Abhinit Srivatsav  Coorg Institute Of Dental Sciences  Dept Of Periodontics And Implantology, Room no. 4 K.K. Campus, Magulla village, Virajpet, Kodagu, Karnataka, 571218 Kodagu KARNATAKA
Kodagu
KARNATAKA 
09535225866

drabhinitsrivatsav@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Coorg institute Of Dental Sciences  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K068||Other specified disorders of gingiva and edentulous alveolar ridge,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Dental Titanium Implant  To evaluate the crestal bone levels and bone density around the dental implant for the crown-implant ratio of less than or equal to 1:1.5.  
Comparator Agent  Dental Titanium Implants  Comparative evaluation of crestal bone levels and bone density between the crown implant ratios of less than or equal to 1:1.5 and more than 1:1.5. 
Intervention  Dental Titanium Implants  To evaluate the crestal bone levels and bone density around the dental implant for the crown-implant ratio of more than 1:1.5.  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  65.00 Year(s)
Gender  Both 
Details  Eighteen years of age to sixty five years of age.
Fully healed bone sites. (at least 6 months after tooth extraction)
No bone augmentation procedures before and during implant placement.
Edentulous gap for at least I implant in any region of the mouth with minimum Imm
distance range from adjacent tooth/teeth.
No medical contraindication for implant surgery.
Edentulous site of implant in any region of the mouth with minimum lmm of mucosal
tissue thickness.  
 
ExclusionCriteria 
Details  Poor oral hygiene.
Symptoms or history of periodontitis or peri-implantitis treatment.
Smoker and alcoholic person.
Patients with systemic diseases.
Alveolar ridges with bone defects at implantation sites.
Absence of attached gingiva or presence less than 2 mm. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Not Applicable 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
Crestal bone levels and bone density, in implant site with crown-implant ratio of less than or equal 1:1.5.  baseline 1 month 3 months
 
 
Secondary Outcome  
Outcome  TimePoints 
Crestal bone levels & bone density, in implant site with crown implant ratio of more than l:1.5.   baseline 1 month 3 months. 
 
Target Sample Size   Total Sample Size="28"
Sample Size from India="28" 
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)   01/04/2026 
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="0"
Months="8"
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   NEED FOR THE STUDY 
One of the successful criteria for implant restorations is the stability of Osseo integration and bone to-implant contact (BIC). It is generally accepted that in physiological functional load can be expected to have a crestal bone loss of to 1.5 mm within the first year and less than 0.2 mm every successive year. According to Hingsammer et al. the ratio between the crown and the implant should not exceed 1.7 in order to avoid increased early bone loss". Prosthetic failure occurred at C/I ratio 1:1.75 and CHS 15 mm. Recent research carried out by Hammerle et al., where it was determined that from a biomechanical point of view, it is desirable for a crown-to-implant ratie to be in the range of 0.9 to 2.2 in single restorations. Increasing this marker above certain limits may lead to mechanical complications due to overloading occlusal forces upon the marginal part of the alveolar bone, crest module and implant body. With its increase, the size of the non axial forces rises, with which the crown acts as a lever arm. This creates a bending moment that carries stress to the marginal bone, It becomes clear that the crown-to-implant ratio should be subject to careful consideration in making the treatment plan in implant recovery. increase in its ratio leads to a proportional rise in the mean stress on the retained screw and peri-implant bone.
 B. Stoichkov, D.Kirov et al indicate that prosthetic restorations with higher crown to-implant ratio tend to cause higher marginal bone loss than those with lower one. in the mandibular molar area. Increasing the ratio of 1:1 to 1.25:1 leads to intensifying the stress in the implant crest module by 30.1%. respectively: in the ratio 1.5:1 the stress is grown by 51.5°%.

 OBJECTIVES OF THE STUDY 
 1. To evaluate the crestal bone levels and bone density around the dental implant for the crown-implant ratio of less than or equal to 1:1.5.
 2. To evaluate the crestal bone levels and bone density around the dental implant for the crown-implant ratio of more than 1:1.5. 
 3. Comparative evaluation of crestal bone levels and bone density between the crown implant ratios of less than or equal to 1:1.5 and more than 1:1.5.


Radiographic parameters to be assessed are:
 1. Edentulous area at implant site. (With CBCT)
 2. Marginal bone levels and bone density around implant with SIDEXIS 4 software with SICATSUITE version 2.0. (Dentsply Sirona; York, US) immediately after prosthesis placement, after I month of prosthesis placement, 3months of prosthesis placement. 

Method:
Marginal bone loss and bone density will be calculatcd by comparing bonc-to-implant contact levels to the radiographic bascline cxamination made with CBCT aken immediately after prosthesis placement.
The following linear measurements between landmarks are taken:  
1) crown height (CH) will be measured from the top of the restoration to the first bone-to implant contact (FBIC) on both mesial and distal sides
2) implant length (|L) will be measured from the apex to the FBIC on both mesial and distal sides. To obtain the mesial CII ratio, the mesial CH is divided by the mesial IL. The distal C/L ratio will also be determined. and mean mesiodistal C/1 ratio is then obtained for each implant. The periimplant marginal bone level will be measured from the reference point to the FBIC. The reference point is the fixture abutment interface. The mesial and distal values of the marginal bone loss are averaged to one value. The mean marginal bone loss will be calculated as the difference between the initial marginal bone level and the marginal bone level at the follow-up examination. 


 
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