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Clinical Trials/NCT07536776
NCT07536776CompletedNot Applicable

Marginal Bone Loss and Retention of Four-Implant Locator-Retained Mandibular Overdentures: 7 Years Follow up

Mansoura University1 site in 1 country27 target enrollmentStarted: January 12, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
27
Locations
1
Primary Endpoint
Marginal Bone Loss by periapical radiography

Study Overview

Brief Summary

ABSTRACT Statement of the problem: Insufficient long-term retrospective data is evaluating marginal bone loss and retention of four-implant Locator-retained mandibular overdentures.

Purpose: To assess marginal bone loss and retention of four-implant Locator-retained mandibular overdentures over seven years at the time of overdenture insertion (T0), 1 year (T1), and 7 years (T7) after insertion.

Material and methods: This retrospective study included 27 completely edentulous patients with maxillary single denture, and four parallel implants were placed interforaminal, and they already have a mandibular four-implant retained overdenture with LOCATOR attachments.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients rehabilitated with a mandibular overdenture retained by four dental implants.
  • •Four implants positioned in the anterior and premolar regions of the mandible. Four Locator attachments used to retain the mandibular overdenture. Availability of baseline clinical and radiographic records at the time of prosthesis insertion.
  • •Availability of clinical and radiographic records at 1-year and 7-year follow-up.

Exclusion Criteria

  • •Patients with incomplete clinical or radiographic records. Patients without the required 1-year or 7-year follow-up records. Patients with radiographs that were inadequate for reliable assessment of peri-implant marginal bone levels.
  • •Patients whose records did not allow assessment of prosthetic retention at the specified follow-up periods.

Arms & Interventions

Implant-Retained Overdenture Group

Experimental

Intervention: implant retained overdenture (Other)

Implant-Retained Overdenture Group

Experimental

Intervention: four dental implant with locator attachment (Device)

Outcomes

Primary Outcomes

Marginal Bone Loss by periapical radiography

Time Frame: From the time of implant loading (Baseline), 1year and 7 years.

Marginal bone loss will be assessed using standardized intraoral periapical radiographs. The vertical distance from the implant reference point to the alveolar bone crest will be measured on the mesial and distal surfaces of each implant. Measurements will be recorded at implant insertion (baseline), 1 year, and 7 years, and the mean value of the four implants will be calculated for each patient.

Secondary Outcomes

  • Prosthetic Retention by a digital force gauge(baseline, 1year and 7 years.)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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