Conventional, Overdenture and Palateless Overdenture Oral Health Impact Comparison Study

University of North Carolina (UNC)

Status: Completed

Conditions: Jaw, Edentulous

Treatments: Device: Overdenture treatment

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT02731703

16-0521

Details and patient eligibility

About

This study will identify and enroll patients already scheduled to receive guided maxillary implant placement with palateless overdenture. Standard clinical practice will be followed for this multi-stage process. The study purpose is to evaluate the degree of satisfaction during the standard progression in order to determine at which post edentulous stage patients achieve maximum satisfaction using the Oral Health Impact Profile 49 (OHIP 49).

Full description

The OHIP 49 will be administered at pre-treatment (edentulous condition) and after each visit (i.e., newly fabricated conventional denture, conversion to a 4 implant retained overdenture and finally a 4 implant retained palateless overdenture). Additionally they will be recalled yearly for 5 years.

Participants will have an interim denture fabricated to be worn for 10-12 weeks. During this time, participants will have 4 implants placed and continue wearing the interim denture. At 8 weeks after implant placement, participants will have locator attachments placed on implants and the interim denture snapped into place, termed the 'overdenture.' After 10-12 weeks of wearing this overdenture, patients will receive a new denture, termed 'final palateless overdenture,' which consists of a denture snapped into the 4 implants without a palate. Participants will be evaluated at a 10-12 week followup from insertion of this prosthesis. Participants will complete questionnaires at each stage of treatment.

One year after delivery of the final palateless overdenture and for five consecutive years patients will be asked to return for a follow up appointment.

Estimated duration of patient participation is approximately 5 years and 8 months (271 weeks). Estimated time for active clinical treatment is 8 months (32 weeks) with understanding of flexibility based on laboratory fabricated denture frameworks and adjustments needed for approval of esthetics.

Enrollment: 14 patients

Sex: All

Ages: 18 to 99 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Capable of giving informed consent
• Able and willing to follow study procedures and instructions
• In good general health
• Edentulous in maxillary arch for a period of at least 6 months
• Have adequate bone volume present to place four maxillary implants without necessity of sinus augmentation or hard and soft tissue grafting ( as determined by the investigator following panoramic radiograph acquisition)

Exclusion criteria

• ASA (American Society of Anesthesiologists) Class 3+
• Immunocompromised (Including HIV infection)
• Current drug abuse (self-reported as part of the School of Dentistry health history
• Pregnant or plans to be pregnant at any point during trial
• History of IV or oral bisphosphonate use contraindicating dental implant therapy
• Chronic disease with oral manifestations
• Exhibit Oral pathology
• Ongoing medications initiated less than three months prior to enrollment (medications for chronic medical conditions must be initiated at least three months prior to enrollment.)
• Smoker within the past 6 months
• Diabetes
• Known allergies to any materials used in denture fabrication or implant surgery

Trial design

14 participants in 1 patient group

Overdenture Treatment

Description:

Guided maxillary implant placement with palateless overdenture

Treatment:

Device: Overdenture treatment