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Clinical Trials/NCT06720389
NCT06720389
Completed
N/A

Effect of Two Different Digital Construction Techniques of Implant-assisted Overdentures: a 3-year Prospective Radiographic Study

Mansoura University1 site in 1 country20 target enrollmentOctober 12, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Peri Implant Bone Loss
Sponsor
Mansoura University
Enrollment
20
Locations
1
Primary Endpoint
peri implant bone loss
Status
Completed
Last Updated
last year

Overview

Brief Summary

twenty patients received mandibular overdenture constructed by different construction techniques were classified equally and randomly into two groups peri implant bone loss was assessed by CBCT at baseline (T0), at1 year(T1), at 3 years(T3) and posterior ridge resorption was assessed by CBCT at baseline (T0), at 1 year( T1), at 3 years (T3). By superimposition of pre and post CBCT.

Detailed Description

twenty patients received mandibular overdenture constructed by different construction techniques were classified equally and randomly into two groups (n = 10 per group): Group A: received milled mandibular overdenture opposed by maxillary complete denture. Group B: received 3D-printed mandibular overdenture opposed by maxillary acrylic complete denture. peri implant bone loss was assessed by CBCT at baseline (T0), at1 year(T1), at 3 years(T3) and posterior ridge resorption was assessed by CBCT at baseline (T0), at 1 year( T1), at 3 years (T3). By superimposition of pre and post CBCT.

Registry
clinicaltrials.gov
Start Date
October 12, 2022
End Date
November 6, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All patient wearing maxillary conventional denture.
  • All patients had temporary mandibular overdenture supported by vertically inserted 4-implant at least six months ago.
  • A Cone Beam Computed Tomography (CBCT) done to verify the accurate position and success of the inserted implant.
  • They were healthy, free from any systemic diseases relating to bone resorption such as uncontrolled diabetics or osteoporosis. This was achieved through medical history and clinical examination by physician.
  • At least 15 mm restorative space must be available (from the mucosa covering the crest of the residual ridge to proposed occlusal plane) to permit construction of all types of tested prosthesis (class I according to Ahuja and Cagna). This was detected by a tentative jaw relation.
  • All patients are of angel's class I maxillo-mandibular relationships.

Exclusion Criteria

  • Patients had head and neck radiotherapy, patients with bleeding disorders or hepatic patients.
  • Patients with metabolic disorders as diabetes mellitus, osteoporosis and hepatic disorders that might affect osseointegration.
  • Long term immunosuppress and corticosteroid drug therapy.
  • Patient with abnormal habits as clenching and bruxism.
  • Smoking patient.
  • Uncooperative patients.
  • Neuromuscular diseases.
  • Patient with problems in TMJ.

Outcomes

Primary Outcomes

peri implant bone loss

Time Frame: at baseline (T0), at1 year(T1), at 3 years(T3)

peri implant bone loss was assessed by CBCT

posterior ridge resorption

Time Frame: at baseline (T0), at 1 year( T1), at 3 years (T3).

posterior ridge resorption was assessed by CBCT at baseline (T0), at 1 year( T1), at 3 years (T3). By superimposition of pre and post CBCT.

Study Sites (1)

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