An Observational Clinical Case Series Study to Assess Fit and Quality of Full Dentures Fabricated by AM

Mouth, Edentulous Clinical Trial

Official title:

An Observational Clinical Case Series Study to Assess Fit and Quality of Full Dentures

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04023006
• Other study ID #: PRPA 22901 / CR 02
• Status: Terminated
• Start date: August 1, 2019
• Est. completion date: April 1, 2020

Study information

• Verified date: February 2021
• Source: Dentsply International
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This observational clinical case series investigation will be conducted on approximately five (5) enrolled subjects at one (1) site in the US. Treatment of subjects encompasses all steps to fabricate new dentures for maxilla and/or mandible. The subjects will be followed 7-10 days after final delivery of the denture

Description:

This investigation is undertaken to evaluate the workflow and concomitant products to create full dentures by using additive manufacturing (AM) technology, i.e. Digital Light Processing™ Technology (Carbon 3D) to restore fully edentulous jaws. The assessment includes quality of materials provided by Dentsply Sirona Lab by using printers for AM (M series, Carbon 3D 1089 Mills Way, Redwood City, CA 94063). This assessment will be done by clinical review of the AM dentures on fit and quality. In addition, the evaluation includes a patient survey to assess current dentures and the new AM dentures with a subjective comparison of both.

The target subjects are male or female, 18 years and older with the need of a full denture in one or both jaws, being completely edentulous. The newly fabricated denture is to replace an existing full denture. For this descriptive study, no minimum number of patients is defined, but to achieve a reasonable subject number, a minimum of five (5) and a maximum of ten (10) patients will be enrolled, i.e. ten to twenty (10-20) denture arches will be fabricated within this study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 10
• Est. completion date: April 1, 2020
• Est. primary completion date: April 1, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subject is 18 years or older.

• Subject has given written consent to participate in the trial.

• Subject is in good general health.

• Subject requires a new removable full denture for both jaws.

• Subject is completely edentulous in the maxilla and mandible.

• Subject is already wearing a full denture in the maxilla and mandible.

• Subject is willing to undergo dental treatment to receive a new full denture for both jaws.

• Subject confirms availability for treatment and all indicated follow-up visits.

Exclusion Criteria:

• Subject is younger than 18 years.

• Subject is pregnant.

• Subject has disabilities that do not allow a regular dental treatment.

• Subject with some systemic medical complications that cause difficulty in impression taking or judging occlusion of device.

• Subject is currently participating in another study.

• Subject has an allergic history regarding materials used in this trial.

• Subject with xerostomia/ dry-mouth syndrome.

• Lack of compliance is expected.

• Those subjects who cannot provide informed consent for any reason

• Acute stomatitis.

• Status after tumor treatment in head-neck region (removal, radiotherapy).

• Acute cancer.

• Incomplete hard and/or soft tissue in the oral cavity.

• Muscle and/or nerve damage in the head-neck region.

• Insufficient vertical height and/or insufficient mouth opening.

• Resilient hyperplastic mucosa ("flappy ridges").

• Bruxism.

• Insufficient oral hygiene. The existing dentures should have no visible calculus.

• Previously enrolled in the present investigation.

• Involvement in the planning and conduct of the clinical investigation. (applies to all Dentsply Sirona & Carbon 3D staff, investigational site staff staff and third party vendor).

Related Conditions & MeSH terms

• Mouth, Edentulous

Intervention

Device:
• Removable prostheses
Full dentures created by Additive manufacturing (Carbon Printers)

Locations

Country	Name	City	State
United States	Boston University Goldman School of Dental MEdicine	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Dentsply International

Country where clinical trial is conducted

United States, 

References & Publications (2)

Celebic A, Knezovic-Zlataric D, Papic M, Carek V, Baucic I, Stipetic J. Factors related to patient satisfaction with complete denture therapy. J Gerontol A Biol Sci Med Sci. 2003 Oct;58(10):M948-53. — View Citation

Schwindling FS, Bömicke W, Hassel AJ, Rammelsberg P, Stober T. Randomized clinical evaluation of a light-cured base material for complete dentures. Clin Oral Investig. 2014;18(5):1457-65. doi: 10.1007/s00784-013-1110-4. Epub 2013 Sep 21. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of the fit of the denture	A questionnaire of assessment of fit by ranking, in comparison to the previous denture, using a Likert Scale from a minimum of 5 to a maximum of 1.; Much worse (5) Worse (4) Same (3) Better (2) Much better (1)	At Final Placement of Denture, through study completion, an average of one month
Secondary	Aesthetics of dentures	A questionnaire of assessment of aesthetics by ranking, in comparison to the previous denture, using a Likert Scale from a minimum of 5 to a maximum of 1.; Much worse (5) Worse (4) Same (3) Better (2) Much better (1)	At Final Placement of Denture,through study completion, an average of one month
Secondary	Function of dentures	A questionnaire of assessment of function by ranking, in comparison to the previous denture, using a Likert Scale from a minimum of 5 to a maximum of 1.; Much worse (5) Worse (4) Same (3) Better (2) Much better (1)	At Final Placement of Denture,through study completion, an average of 1 month
Secondary	Dentist's satisfaction with treatment: questionnaire	A questionnaire of assessment of satisfactions of treatment by ranking, in comparison to the previous placed denture, using a Likert Scale from a minimum of 5 to a maximum of 1.; Much worse (5) Worse (4) Same (3) Better (2) Much better (1)	At Final Placement of Denture, through study completion, an average of 1 month