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Clinical Trials/NCT06166446
NCT06166446
Completed
N/A

Comparison of Denture Base Adaptation and Per-implant Tissue Health Between CAD and CAM Implant Retained Complete Overdenture

Mansoura University1 site in 1 country15 target enrollmentJanuary 15, 2022
ConditionsPeriimplantitis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Periimplantitis
Sponsor
Mansoura University
Enrollment
15
Locations
1
Primary Endpoint
Modified Plaque Index
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Background: Complete overdenture manufacturing has been greatly developed using computer-aided designing and computer-aided manufacturing (CAD-CAM) technology.

Material and method: 15 completely edentulous patients, divided into two groups, received two implants in the mandibular canine area with ball attachment. The first group received a CAD/CAM-milled mandibular overdenture and a maxillary acrylic conventional complete denture, while the second group received a 3D-printed mandibular overdenture and a maxillary acrylic complete denture. Peri-implant soft tissue and denture adaptation were evaluated using clinical parameters

Detailed Description

Background: In recent years, complete overdenture manufacturing has been greatly developed using computer-aided designing and computer-aided manufacturing (CAD-CAM) technology. This clinical study compared the soft tissue health between CAD/CAM-milled and 3D-printed implants that retained complete overdentures. Material and method: 15 completely edentulous patients, divided into two groups, received two implants in the mandibular canine area with ball attachment. The first group received a CAD/CAM-milled mandibular overdenture and a maxillary acrylic conventional complete denture, while the second group received a 3D-printed mandibular overdenture and a maxillary acrylic complete denture. Peri-implant soft tissue was evaluated using clinical parameters including the gingival index, plaque index, bleeding index, and probing depth at the time of mandibular complete overdenture insertion (T0), six months (T6), and twelve months (T12) of denture use.

Registry
clinicaltrials.gov
Start Date
January 15, 2022
End Date
February 2, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • poor denture adaptation co-operative patients

Exclusion Criteria

  • metabolic diseases uncontrolled diabetes osteoporosis and hyperparathyroidism.

Outcomes

Primary Outcomes

Modified Plaque Index

Time Frame: 12 months

a calibrated pressure sensitive plastic periodontal probe, the distance between marginal border of the peri-implant mucosa and the tip of the probe was measured and considered as pocket depth

Study Sites (1)

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