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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06166446
Other study ID # A10080921
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 15, 2022
Est. completion date February 2, 2023

Study information

Verified date November 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date February 2, 2023
Est. primary completion date April 25, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 58 Years to 68 Years
Eligibility Inclusion Criteria: poor denture adaptation co-operative patients Exclusion Criteria: metabolic diseases uncontrolled diabetes osteoporosis and hyperparathyroidism.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
subtractive technique
The milled denture teeth are then bonded into the milled recesses using a special PMMA bonding system.
additive technique
The denture teeth were printed as one unit using the same method with tooth resin (DENTCA Denture Tooth, Shade A2).

Locations

Country Name City State
Egypt Mansoura university Mansoura

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Emera RMK, Shady M, Alnajih MA. Comparison of retention and denture base adaptation between conventional and 3D-printed complete dentures. J Dent Res Dent Clin Dent Prospects. 2022 Summer;16(3):179-185. doi: 10.34172/joddd.2022.030. Epub 2022 Nov 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Modified Plaque Index 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 12 months
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