Skip to content

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.

A Randomized Controlled Trial: To Assess the ability of surgical guide fabricated using CAD-CAM with and without metallic sleeve to accurately replicate the planned position of dental implant when placed surgically in the adult patients. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063475
Enrollment
24
Registered
2024-03-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Metal Free Surgical Guide. : The surgical guide for implant placement will be completely devoid of metal. Time duration- 1 week timeline. Control Intervention1: Surgical guide with Meta

Sponsors

Dr Poonjee Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
1.To Evaluate & compare the Vertical & Horizontal Position of implant placed using Surgical guide with and without metallic sleeve. 2.To investigate the metallic sleeve surface changes seen after the surgical implant placement using Surgical guide with metallic sleeve. Timepoint: Time of duration - 2 years

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Narendra Padiyar

Mahatma Gandhi Dental College and Hospital

drnpadiyaru@gmail.com9928561339

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026