A clinical study to evaluate the ability of surgical guides with and without metallic sleeves in replicating the pre-planned dental implant position in adult patients.
- Registration Number
- CTRI/2024/03/063475
- Lead Sponsor
- Dr Poonjee Gupta
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
a.Participants with minimum age limit of 18 years of either sex.
b.Participants who are partially edentulous tooth supported (Kennedy’s Class III and IV) with one or more teeth missing (from incisor to 1st molar) in either or both sides of upper or lower or both jaws.
c.Participants with completely healed partial edentulous area.
d.Participants with adequate mouth opening for purposed surgical procedure.
e.Participants with ASA Category I and II.
f.Participants who have given consent for dental implant as their choice of treatment for replacing missing tooth/teeth.
a.Participants suffering from active periodontal disease with mobility in the remaining teeth .
b.Participants with Kennedy’s Class I and Class II edentulous situation.
c.Participants having H/O bruxism.
d.Participants having H/O tumour, radiation exposure or bone diseases in the area of planned implant site.
e.Participants allergic to metals.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To Evaluate & compare the Vertical & Horizontal Position of implant placed using Surgical guide with and without metallic sleeve. <br/ ><br> <br/ ><br>2.To investigate the metallic sleeve surface changes seen after the surgical implant placement using Surgical guide with metallic sleeve. <br/ ><br>Timepoint: Time of duration - 2 years
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI