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Clinical Assessment of CAD/CAM Monolithic Complete Denture

E

Eman Assam

Status

Completed

Conditions

Complete Denture

Treatments

Device: Conventional denture
Device: CAD/CAM monolithic denture

Study type

Interventional

Funder types

Other

Identifiers

NCT07091552
9208697

Details and patient eligibility

About

The aim of the study is to evaluate trueness, tooth position, retention, and patient satisfaction of CAD/CAM monolithic complete denture

Enrollment

22 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Completely edentulous patients, and willing to participate and sign the informed consent.
  • No cognitive or psychological deficits.
  • Moderate arch size with moderate undercut.
  • No retrognathic or prognathic jaw relationship. (Normal horizontal ridge relationship)

Exclusion criteria

  • Participants having undercuts, flabby ridge, severely resorbed ridges.
  • Participants with noticeably poor neuromuscular control, hyposalivation, general health, or other issues rendering repeated appointments difficult.
  • Oral mucosa exhibits papillary hyperplasia or pathologic changes

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

22 participants in 2 patient groups

CAD/CAM monolithic denture
Experimental group
Treatment:
Device: CAD/CAM monolithic denture
Conventional denture
Active Comparator group
Treatment:
Device: Conventional denture

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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