Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03198520
Other study ID # DS002
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 6, 2017
Est. completion date October 7, 2019

Study information

Verified date November 2020
Source Solvay Dental 360
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the change in patient Oral Health-related Quality of Life (OHRQoL) from wearing a cobalt chrome (CoCr) removable partial denture (RPD) to wearing the Solvay Dental 360TM polymer Removable Partial Denture (RPD) for 8 weeks.


Description:

Cohort study conducted in the United States & United Kingdom to assess Oral Health Related Quality of Life (OHRQoL) in patients receiving the study polymer Removable Partial Denture (RPD) as compared to their baseline Cobalt Chrome (CoCr) Removable Partial Denture (RPD) Oral Health Quality of Life (OHRQoL).


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date October 7, 2019
Est. primary completion date October 7, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - with the absence of 3 or less teeth per saddle, excluding third molars - partial denture in one arch only - with previous denture wearing experience, and Cobalt Chrome (CoCr) Removable Partial Denture (RPD) fitted in the previous 24 months and the patient is currently and routinely wearing the denture - With a stable oral health in terms of absence of disease activity affecting the periodontium, dental hard tissues (caries), pulp and the structural/aesthetic integrity of restored teeth - With at least 1 posterior natural tooth occlusal stop (molar or premolar) - Class I, Class II and Class III (Kennedy's Classification) - Occlusal spacing (static and dynamic) around clasp assembly including the occlusal rest Exclusion Criteria: - Patients requiring extensive treatment prior to the provision of a removable partial denture (RPD) - Patients with active primary disease; caries, periodontal disease or symptoms of pulpal or apical pathology to the remaining teeth - Patients with irreversibly compromised structural/aesthetic integrity of restored teeth that cannot be restored as part of the provision of treatment. - Patients with an opposing Removable Partial Denture (RPD). Removable Partial Denture (RPD) to only be in one arch and must oppose a full denture or a dentate arch which provides a stable occlusal relationship - Canines are NOT to be replaced with the Removable Partial Denture's (RPDs). Patients must have their natural canines present

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Solvay Dental 360™
polymer Removable Partial Denture (RPD)

Locations

Country Name City State
United Kingdom Leeds School of Dentistry Unversity of Leeds Leeds West Yorkshire
United States The University of Illinois Chicago College of Dentistry Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Solvay Dental 360

Countries where clinical trial is conducted

United States,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Patient Oral Health-related Quality Subjects conducted the Oral Health-related Quality of Life (OHRQoL) before and after wearing the Solvay Dental 360™ polymer Removable Partial Denture (RPD). OHRQoL is a multidimensional survey which can be defined as a person's assessment of how functional, psychological, social factors, pain, or discomfort affect his/her well-being in the context of oral health. The purpose of the survey is to evaluate the change in these factors from wearing a cobalt chrome (CoCr) removable partial denture (RPD) to wearing the Solvay Dental 360™ polymer Removable Partial Denture (RPD).
This score is calculated by a summation of the score from each question; each having the following scoring:
Response Score Never 0 Points Hardly Ever 1 Point Occasionally 2 Points Fairly Often 3 Points Very Often 4 Points
It ranges from 0 to 56 points. The overall scores are from the baseline Cobalt Chrome (CoCr) RPD and 8 weeks for Polymer RPD. Lower scores are better outcomes.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and 8 weeks for Polymer Removable Partial Denture
Secondary Comparison of Health of Abutment Teeth To investigate the difference in health of the abutment teeth following the use of the polymer RPD as compared to the CoCr RPD as assessed by the plaque score and gingival bleeding index.
The plaque score is determined by assessing each tooth and the amount of plaque on the individual surfaces. The total number of plaque containing surfaces is divided by the total number of surfaces per arch of the mouth.
Arch plaque is a subset of the whole plaque score calculated as the number of arch surfaces with plaque divided by the number of arch surfaces assessed.
The gingival bleeding index is a designation of the degree of inflammation, as determined by a "bleeding on probing" assessment. Each tooth is probed at six sites and the bleeding is scored as present or absent. The number of sites where the bleeding is noted is divided by the total number of surfaces evaluated.
All assessments are expressed as a percentage and an increased percentage indicates a poorer patient outcome.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and 8 weeks for the Solvay Dental 360™: Polymer Removable Partial Denture
Secondary Operator Assessment Operator assessment of the adaptation of the polymer frame, adaption of the tissue base areas and their relationship to the frame adaptation, functional evaluation, aesthetic assessment and oral health assessment of abutment teeth and the periodontium. This assessment was done with a Likert scale at baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and visits 5, 6, 7 and 8 for the Solvay Dental 360™: Polymer Removable Partial Denture.
This assessment of aesthetics was determined by the operator based on a five point scale rating from very dissatisfied through very satisfied. More satisfied is a better outcome.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and visits 5 (5 weeks), 6 (6 weeks), 7 (7 weeks) and 8 (8 weeks) for the Solvay Dental 360™: Polymer Removable Partial Denture
Secondary Patient Frame Preference Patient-centered assessment of preference at the final visit for the study.
Patients were asked to choose their preference of Removable Partial Denture based on comfort, aesthetics and chewing. Preference for a specific denture is a better outcome.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and 8 weeks for the Solvay Dental 360™: Polymer Removable Partial Denture
Secondary Review for Mechanical Failure This is an evaluation of the Solvay Dental 360™ Polymer Removable Partial Denture (RPD) for chips, cracks, fractures, permanent deformation or other signs mechanical failure. The number in the reported data represents a cumulative number of Solvay Dental 360™Polymer Removable Partial Denture (RPD) devices with these mechanical failures.
A device deficiency was defined as "the inadequacy of a medical device with respect to its identity, quality, durability, reliability, safety or performance."
Approximately 8 weeks
Secondary Operator Assessment of Pocket Depth Oral Health parameters associated with the Removable Partial Denture (RPD) on pocket depths based on Operator assessment.
Pocket depths are expressed in mm increments for mesial, mid, and distal locations on the lingual and buccal surfaces of the tooth. To measure pocket depth, a probe is placed beside the tooth beneath the gumline and indicates the groove between the gums and teeth. Visit 2 with the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) is compared to visit 8 with the Solvay Dental 360™: Polymer Removable Partial Denture. In general, pocket depths of 1 to 3 mm indicate a healthy mouth and 4mm and greater may indicate periodontitis. The score is calculated as an average of all depths reported for all surfaces assessed.
A lower score is a better outcome.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and 8 weeks for the Solvay Dental 360™: Polymer Removable Partial Denture
Secondary Oral Health Parameters: Operator Assessment of Mobility: Oral Health parameters associated with the Removable Partial Denture (RPD) abutment teeth and Removable Partial Denture (RPD): mobility (measured as a categorical value of either Class I, Class II or Class III).
Mobility of the teeth abutting the missing tooth as well as adjacent to the abutment tooth are classified via the Miller Classification as the following:
Class I: Tooth can be moved less than 1mm in the buccolingual or mesiodistal direction; this included no mobility
Class II: Tooth can be moved 1mm or more in the buccolingual or mesiodistal direction. No mobility in the occlusoapical direction (vertical mobility)
Class III: Tooth can be moved 1mm or more in the buccolingual or mesiodistal direction. Mobility in the occlusoapical direction is also present
The mobility score assessment is noted as proportion of teeth that moved from a lower classification to a higher classification. Class I is a better outcome.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and 8 weeks for the Solvay Dental 360™: Polymer Removable Partial Denture
Secondary Oral Health Parameters: Mucosal Bearing Areas Oral Health parameters associated with the Solvay Dental 360™ Removable Partial Denture (RPD): mucosal bearing areas (measured as an evaluation of bleeding on probing indicated as a categorical value of "bleeding present" or "bleeding absent", as compared to the Cobalt Chrome (CoCr) Removable Partial Denture (RPD).
Operators were asked to rate the health of the mucosal bearing areas as poor, fair or good. The mucosal bearing area is the cushion between the denture base and the supporting bone. Good is a better outcome.
Baseline for the Cobalt Chrome (CoCr) Removable Partial Denture (RPD) and 8 weeks for the Solvay Dental 360™: Polymer Removable Partial Denture
See also
  Status Clinical Trial Phase
Recruiting NCT06007365 - Post Market Clinical FoIIow up (PMCF) Medical Device (MD) of Z-Systems Monotype Zirconia Dental Product: Z5m Dental Implants Registry
Completed NCT05350293 - Evaluation of the Abutment Type Following Oral Implants in Terms of the Surrounding Bone Height N/A
Completed NCT05650099 - Peri-implant Health of Dental Implants in the Posterior Region; an Evaluation After 10 Years
Completed NCT05359549 - Dental Implant Treatment for Two Adjacent Teeth in the Maxillary Aesthetic Region: an Evaluation After 10 Years
Completed NCT02239718 - Novel Use of 2-unit Cantilever Resin-bonded Bridges for Replacing Missing Molar Teeth - a Randomized Clinical Trial N/A
Recruiting NCT04581304 - The Use of Bio-Oss Collagen for Sinus Augmentation Using the Transcrestal Approach. N/A
Not yet recruiting NCT06033989 - Clinical and Radiographic Evaluation of the Effect of Hyaluronic Acid Surface Treatment Versus Sandblasted Acid Etched on Stability of Delayed Dental Implant in Posterior Maxilla. N/A
Completed NCT06178796 - Evaluation of the Effect of the Gap Between Bone and Implant Surface on the Implants Stability N/A
Recruiting NCT05649085 - Evaluation of Single-unit Implant-supported Prostheses Survival Using CoCr Prosthetic Abutments: Prospective Observational Study
Completed NCT02123420 - Platform Switching vs Regular Platform Implants. One Year Results From a RCT N/A
Active, not recruiting NCT05362591 - Anterior Resin Bonded Restorations for Adolescent N/A
Active, not recruiting NCT04378140 - Retention and Durability of the Anterior Zirconia Wing Bridge
Completed NCT01953991 - OHQoL With Removable Partial Dentures; a Pilot Study N/A
Active, not recruiting NCT01229995 - Randomized Controlled Clinical Trial of CAD/CAM and Conventionally Fabricated Singl Implant Abutments. N/A
Recruiting NCT04908618 - The Accuracy of Conventional Versus Digital Implant Impression Techniques N/A
Completed NCT05476848 - Relationship Between Oral Findings and Salivary Factors in Sars-Cov-2 Patients N/A
Completed NCT05403099 - Effect of Topical Application of Hyaluronic Acid on Stability of Immediate Loading Dental Implant in Posterior Maxilla N/A
Active, not recruiting NCT06334081 - Different Surgical Drilling Protocols in Posterior Maxilla N/A
Completed NCT03877419 - Comparison of Different Drilling Speed to Classify Bone Quality by Tactile Sensation on a Saw Bone Model
Recruiting NCT05089214 - ONE-1 Oral graNd Est 1 N/A