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CTRI Number  CTRI/2026/03/106566 [Registered on: 19/03/2026] Trial Registered Prospectively
Last Modified On: 19/03/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Preventive
Dentistry 
Study Design  Non-randomized, Active Controlled Trial 
Public Title of Study   Comparing tooth contact in natural teeth and dental implants. 
Scientific Title of Study   A split mouth clinical study on comparison of proximal contact tightness with implant supported prosthesis and natural tooth contacts 
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 Moghal Wasim Baig 
Designation  MDS STUDENT 
Affiliation  Uttaranchal Dental and Medical Research Institute  
Address  Room No 3 Department of Prostodontics , Crown and bridge Uttaranchal Dental and Medical Research Institute Marzi Grand NH72 Dehradun UK 248140

Dehradun
UTTARANCHAL
248140
India 
Phone  7601053345  
Fax    
Email  wasimmoghalbaig782@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Neha Anand  
Designation  READER 
Affiliation  Uttaranchal Dental and Medical Research Institute  
Address  Room No 3 Department of Prostodontics , Crown and bridge Uttaranchal Dental and Medical Research Institute Marzi Grand NH72 Dehradun UK 248140

Dehradun
UTTARANCHAL
248140
India 
Phone  8758096740  
Fax    
Email  drnehakhaire@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Moghal Wasim Baig 
Designation  MDS STUDENT 
Affiliation  Uttaranchal Dental and Medical Research Institute  
Address  Room No 3 Department of Prostodontics , Crown and bridge Uttaranchal Dental and Medical Research Institute Marzi Grand NH72 Dehradun UK 248140

Dehradun
UTTARANCHAL
248140
India 
Phone  7601053345  
Fax    
Email  wasimmoghalbaig782@gmail.com  
 
Source of Monetary or Material Support  
UTTARANCHAL DENTAL AND MEDICAL RESEARCH INSTITUTE  
 
Primary Sponsor  
Name  Uttaranchal Dental and Medical Research Institute 
Address  Uttaranchal Dental and Medical Research Institute Mazri Grand Haridwar Road NH72 Dehradun UK 248140 
Type of Sponsor  Research institution 
 
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 
Moghal Wasim Baig  UTTARANCHAL DENTAL AND MEDICAL RESEARCH INSTITUTE  room no 3 Department of prosthodontics , Crown and Bridge Uttaranchal Dental and Medical Research Institute NH72 Deharadun UK 248140
Dehradun
UTTARANCHAL 
7601053345

wasimmoghalbaig782@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Committee Uttaranchal Dental and Medical Research Institute  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  systemically healthy individuals with edentulous site in the premolar or molars region  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  comparator   natural tooth proximal contacts  
Intervention  primary intervention  placement of implant- supported prosthesis  
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Patients requiring Implant supported prosthesis in one quadrant posterior region. Natural tooth – natural tooth proximal contacts in the contralateral quadrant .Good oral hygiene & periodontal health .Functional occlusion with no para functional habits. Patients willing to give informed consent. 
 
ExclusionCriteria 
Details  Active periodontal disease & tooth mobility. History of orthodontic treatment with in last 6 months. Those who are immuno-compromised. Those taking drugs known to improve the healing of wounds and bone. Adjacent teeth have an apical pathology. People who smoke. People who deny informed consent. Patient with bruxism (or) other parafunctional habits. 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Difference in proximal contact tightness (in Newtons) between implant-supported prosthesis and adjacent natural tooth contacts measured using a digital force gauge.  BASELINE,1,3 and 6 months. 
 
Secondary Outcome  
Outcome  TimePoints 
NIL  NIL 
 
Target Sample Size   Total Sample Size="20"
Sample Size from India="20" 
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)   30/03/2026 
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="1"
Months="6"
Days="0" 
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   This  split-mouth clinical study aims to compare proximal contact tightness between implant-supported prostheses and adjacent natural tooth contacts. Proximal contact tightness will be objectively measured using a digital force gauge at baseline (time of prosthesis insertion), 1 month, 3 months, and 6 months. The primary outcome is the difference in contact tightness between implant-supported prosthesis and natural teeth over time, while the secondary outcome is the presence of proximal contact loss during follow-up. Adult patients aged 20–60 years requiring a  implant-supported prosthesis with adjacent natural teeth will be recruited. By evaluating changes in contact tightness over multiple time points, this study aims to provide clinical evidence on contact stability around implant restorations. The findings may help clinicians improve proximal contact design, reduce complications such as food impaction and patient discomfort, and enhance the long-term success and maintenance of implant-supported prostheses. 
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