Adams School of Dentistry
Chapel Hill, North Carolina, 27599, United States
Location contact
Vivia Sequeira
CONTACT
NCT Number: NCT07586774
This is a two-armed, single-center clinical study evaluating performance, efficacy and safety of three dimensional (3D) printed complete dentures and milled complete dentures during a 5-year follow-up period. The primary objective of this clinical investigation is to evaluate survival rate, i.e. subjects with survived dentures in both upper and lower jaw, of 3D printed complete dentures and milled complete dentures after 1 year (in each of the groups separately).
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Chapel Hill, North Carolina, 27599, United States
Vivia Sequeira
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Consisting of the following parts:
Consisting of the following parts:
Time frame: One year after baseline (baseline = final denture insertion performed within 6-months from day 1)
Restorations still in function after 1 year.
Time frame: 3 and 6 months, and 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Restorations still in function after 3 and 6 months, and 2, 3, 4 and 5 years.
Time frame: 3 and 6 months, and 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
A denture will be considered successful if all the following criteria are fulfilled:
Absence of major technical complications.
Absence of major biological complications.
Functional occlusion and mastication, assessed by clinical examination and OHIP-EDENT.
Absence of patient reported discomfort, assessed by OHIP-EDENT.
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Evaluation of accuracy of 3D printing and milling technology will be made using Geomagic Software at time of final denture insertion. The denture intaglio at insertion will be compared with the final impression as reference scan.
Time frame: 3 and 6 months, and 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Retention force of the dentures will be evaluated by applying a dynamometer gauge at the following locations: Post dam, Tuberosities and retromolar pads.
Time frame: At baseline, 3 and 6 months, and 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Complications will be recorded and assessed as either:
Time frame: At baseline, 3 and 6 months, and 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Occurrence of biological complications. Biological complications will be evaluated by recording major and minor biological complications. The evaluation of biological complications will be derived from the adverse event (AE)/adverse device effect (ADE) sections of the Case Report Form.
Time frame: 3 and 6 months, and 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Quality of Life through Oral Health Impact Profile for Edentulous Patients (OHIP-EDENT) Questionnaire completed by participating subjects. OHIP-EDENT contains 19 questions, divided into six domains: Functional limitations, Physical pain, Psychological discomfort, Physical disability, Psychological disability and Handicap. Response categories for all questions: 4 = very often; 3 = fairly often; 2 = occasionally; 1 = hardly ever; 0=never, i.e. lower scores corresponds with higher quality of life.
Time frame: 3 and 6 months, and 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Patient satisfaction including aesthetics as evaluated by patient questionnaire including the following questions:
Patient satisfaction with dentures will be evaluated using a likert scale, ranging from 0 to 10 for each of above questions. The likert scale representing a spectrum of feelings between extremes with 0= Very unsatisfied and 10= Very satisfied. Patients will rate their assessment by marking a number corresponding to their feelings at the time. A low score represents a high degree of dissatisfaction, and a high score a high degree of satisfaction
Time frame: At baseline and 3 and 6 months, 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Serial comparison of follow-up denture scans using TRIOS Compare with post insertion adjusted denture scan as reference. Volumetric loss measured in mm3.
Time frame: At baseline and 3 and 6 months, 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Serial comparison of follow-up denture scans using TRIOS Compare with post insertion adjusted denture scan as reference. Maximum vertical loss measured in μm.
Time frame: At baseline and 3 and 6 months, 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Discolouration (intrinsic or interfacial) measured with spectrophotometer. The colour at a central incisor (#8) and the denture just above #8 will be measured.
Time frame: At baseline and 3 and 6 months, 1, 2, 3, 4 and 5 years after baseline (baseline = final denture insertion performed within 6-months from day 1)
Number of occlusal contacts using articulating paper will be documented.
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Appropriateness of tooth shape assessed by the following Yes/No question:
Appropriate Tooth Shape to match facial aesthetics?
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Appropriateness of tooth size assessed by the following Yes/No question:
Appropriate Tooth Size to match facial aesthetics?
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Appropriateness of tooth arrangements assessed by the following Yes/No questions:
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Appropriateness of tooth colour /colour match assessed by the following Yes/No questions:
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Appropriateness of denture base assessed by the following Yes/No questions:
Time frame: At baseline (baseline = final denture insertion performed within 6-months from day 1)
Lip support assessed by the following Yes/No questions:
Time frame: From Day 0 up to completion of the 5-year follow-up visit, on average 5 years and 3 months.
Adverse Events, Adverse Device Effects, and Device Deficiencies spontaneously reported, and collection at each clinical investigation visit.
Contact information is provided by the study sponsor or research team.
Ada Saltarski
CONTACT
Ulrika Bonander
CONTACT
Dentsply Sirona Implants and Consumables
Industry
An Open, Single-center, Prospective, Randomized, Two-armed, Interventional, Post-market Clinical Investigation of 3D Printed Complete Dentures and Milled Complete Dentures During a 5-year Follow-up Period
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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