Mandibular Single Implant Overdenture: a Prospective Clinical Trial

Edentulous Clinical Trial

Official title:

Patient Satisfaction and Clinical Outcomes Following Mandibular Single-implant-retained Overdenture Treatment in Residents of Nursing Homes: a Prospective Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01421849
• Other study ID #: 2011/381
• Status: Withdrawn
• Phase: N/A
• Start date: August 2011
• Est. completion date: December 2015

Study information

• Verified date: December 2022
• Source: University Hospital, Ghent
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study hypothesis: that there would be no difference in patient satisfaction among institutionalised older people before and after treatment with a mandibular single implant-retained overdenture.

In a preliminary phase, a new denture is made or the old denture is adapted to provide a well-fitting denture.

Eight weeks after insertion of the new denture a single implant is placed in the centre of the mandibula. If the level of primary stability is sufficient to enable the implant to resist micromovement, the implant is immediately loaded . If not, the implant is loaded after 6 to 12 weeks. Primary stability is assessed by the final seating torque and by the clinician's interpretation and tactile sense of primary stability. Before, during and after the treatment patient satisfaction and clinical outcomes are evaluated by a 20 item questionnaire and a clinical examination.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2015
• Est. primary completion date: December 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 70 Years to 90 Years

Eligibility

Inclusion Criteria:

• Edentulous residents of nursing homes treated in the mobile dental unit 'Gerodent'.

• They have to be willing to commit to 1.5 year of participation in the study.

• They have to be edentulous for at least one year before starting the implant procedure.

Exclusion Criteria:

• Medical conditions contraindicating implant surgery (unregulated diabetes type II, bisphosphonates)

• History of radiotherapy in the head and neck region

• Insufficient bone for an implant of at least 10 mm length and 4 mm diameter

• Previously treated with dental implants

Related Conditions & MeSH terms

• Edentulous
• Mouth, Edentulous

Intervention

Procedure:
• Denture implantation
In a preliminary phase, a new denture is made according to standardized prosthodontic protocol or the old denture is adapted to provide a well-fitting denture. Eight weeks after insertion of the new denture an implant is placed under local anaesthetics in the centre of the mandibula.If primary stability is good, the implant is immediately loaded by the denture. If not, the implant is loaded after 6 to 12 weeks. Before, during and after the treatment patient satisfaction is evaluated by a 20 item questionnaire. Afterwards questionnaires are compared. After the insertion of the implant clinical evaluations take place at several moments. The total duration of the study will be 12 to 18 months.

Locations

Country	Name	City	State
Belgium	University Hospital Ghent	Ghent

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital, Ghent	Southern Implants, South Africa

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient satisfaction after insertion of the new complete dentures.	This will be measured by a questionnaire with 20 items.	1 week after insertion of the new complete dentures.
Primary	Patient satisfaction after insertion of the complete dentures.	This will be measured by a questionnaire with 20 items.	8 weeks after insertion of the complete dentures.
Primary	Patient satisfaction post-surgical.	This will be measured by a questionnaire with 20 items.	1 week post-surgical.
Primary	Patient satisfaction after surgical procedure, functional loading.	This will be measured by a questionnaire with 20 items.	6-8 weeks after surgical procedure.
Primary	Patient satisfaction after loading the implant.	This will be measured by a questionnaire with 20 items.	1 week after loading the implant.
Primary	Patient satisfaction after loading.	This will be measured by a questionnaire with 20 items.	1 months after loading.
Primary	Patient satisfaction after loading.	This will be measured by a questionnaire with 20 items.	6 months after loading
Primary	Patient satisfaction after loading.	This will be measured by a questionnaire with 20 items.	1 year after loading
Secondary	Implant level : lost implants, loose implants, …		From the first week post-surgical to 1 year after loading.
Secondary	Soft tissue level : Peri-implant inflammation, bleeding index, probing depth		From the first week post-surgical to 1 year after loading.
Secondary	Denture related: soft tissue problems.		From 1 week after insertion of the new complete dentures to 6 months after loading.
Secondary	Repair management: type (fracture, matrix replacement, patrix activation, mechanical problems of the abutment, replacement of denture, relining, adjustment without adding new material) and number.		From 8 weeks after insertion of the complete dentures to 6 months after loading.
Secondary	Maintenance - oral hygiene: Implant abutment: plaque index according to Mombelli, presence of calculus.		From 1 week after loading the implant to 6 months after loading.
Secondary	Maintenance - oral hygiene: Dentures using the denture plaque index by Augsburger and Elahi.		From 8 weeks after insertion of the complete dentures to 6 months after loading.

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