| 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
|
|
|
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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