Clinical Trials Directory

Trials / Completed

CompletedNCT06720389

Effect of Two Different Digital Construction Techniques of Implant-assisted Overdentures

Effect of Two Different Digital Construction Techniques of Implant-assisted Overdentures: a 3-year Prospective Radiographic Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Mansoura University · Academic / Other
Sex
All
Age
50 Years – 65 Years
Healthy volunteers
Accepted

Summary

twenty patients received mandibular overdenture constructed by different construction techniques were classified equally and randomly into two groups peri implant bone loss was assessed by CBCT at baseline (T0), at1 year(T1), at 3 years(T3) and posterior ridge resorption was assessed by CBCT at baseline (T0), at 1 year( T1), at 3 years (T3). By superimposition of pre and post CBCT.

Detailed description

twenty patients received mandibular overdenture constructed by different construction techniques were classified equally and randomly into two groups (n = 10 per group): Group A: received milled mandibular overdenture opposed by maxillary complete denture. Group B: received 3D-printed mandibular overdenture opposed by maxillary acrylic complete denture. peri implant bone loss was assessed by CBCT at baseline (T0), at1 year(T1), at 3 years(T3) and posterior ridge resorption was assessed by CBCT at baseline (T0), at 1 year( T1), at 3 years (T3). By superimposition of pre and post CBCT.

Conditions

Interventions

TypeNameDescription
RADIATIONperi implant bone loss was assessed by CBCTusing CBCT, vertical bone loss (VBL) was measured at baseline (T0), at1 year(T1), at 3 years(T3)
OTHERposterior ridge resorption was assessed by CBCTposterior ridge resorption was assessed by CBCT at baseline (T0), at 1 year( T1), at 3 years (T3). By superimposition of pre and post CBCT.

Timeline

Start date
2022-10-12
Primary completion
2024-08-04
Completion
2024-11-06
First posted
2024-12-06
Last updated
2024-12-18

Locations

1 site across 1 country: Egypt

Regulatory

Source: ClinicalTrials.gov record NCT06720389. Inclusion in this directory is not an endorsement.