Crestal Bone Loss in Mandibular Telescopic Overdentures. Overdenture with Milled Titanium, Milled Poly-ether Ketone Ketones and 3D Printed Chrome Cobalt Secondary Copings.
- Conditions
- Telescopic OverdenturesDental ImplantsCustomized Abutments
- Registration Number
- NCT06639893
- Lead Sponsor
- Cairo University
- Brief Summary
The objective of this clinical trial is to evaluate crestal bone loss every three months at time of overdenture insertion, 3, 6, 9, 12 months from overdenture use. Also, to evaluate prosthesis satisfaction.
All participants will receive conventional complete dentures, followed by two intraforaminal implants. After healing time, fabrication of secondary copings in all cases according to randomized groups for final overdenture insertion.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- Sufficient remaining bone in height, width and thickness in the interforaminal area to allow installation of at least 3.3 mm diameter and 8 mm length implants.
- Adequate amount of interarch space of at least 12mm.
- Age range from 55 to 75 years old age.
- Systemic and metabolic diseases that may affect osseointegration.
- Patients receiving bisphosphonates therapy.
- Patients under radiotherapy or chemotherapy.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Crestal bone loss. one year The aim of this study was to evaluate crestal peri implant bone loss in mandibular telescopic implant retained overdenture with milled titanium, milled poly-ether ketone ketones and 3D printed chrome cobalt secondary copings. Crestal bone loss evaluated every three months using standardized digital periapical radiograph at time of overdenture insertion, 3, 6, 9, and after 12 months from overdenture use.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
EL Minia University
🇪🇬El minia, Egypt