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Effect Of Occlusal Materials Used For All On Four Mandibular Implant Prosthesis With PEEK Framework

M

Mansoura University

Status

Completed

Conditions

Occlusal Trauma

Treatments

Procedure: visio-lign nano composite
Procedure: zirconia crowns
Procedure: peek framework
Procedure: dental implants

Study type

Interventional

Funder types

Other

Identifiers

NCT06159530
A03021121

Details and patient eligibility

About

This study was performed to compare between the effects of different occlusal materials used for all on four implant supported mandibular fixed prosthesis with PEEK framework.

Methods of Evaluation

1- Occlusal force analysis using digital occlusal device (occluscan).

The evaluation periods will be done at time of insertion (T0),6 month (T1),12 month(T2) and 18 month(T3) after framework insertion.

Full description

thirty completely edentulous patients will be selected for the study from the outpatient's clinic of Prosthodontic Department, Faculty of Dentistry, Mansoura University.

The patients will be selected according to the following criteria:

  1. lack of satisfaction of mandibular conventional dentures due to denture instability.
  2. Atrophy of mandibular ridges with insufficient bone.
  3. They were healthy, free from any systemic diseases relating to bone resorption.
  4. All patients have sufficient inter-arch space >15 mm.
  5. Maxillary and mandibular residual alveolar ridges covered by healthy non-inflamed mucosa with even compressibility.
  6. Normal maxilla-mandibular relationship (class I Angle's classification).
  7. All patients will have mandibular bone height not less than 8-10mm as verified by cone beam CT.
  8. Sufficient inter-arch space not less than 23 mm as verified by tentative jaw relation. And restorative space not less than14 mm as verified by putty index technique.

Exclusion criteria included:

1- Systemic disorders affecting bone (such as uncontrolled diabetes mellitus and osteoporosis).

2- Local or general contraindication for surgical procedures. 3- History of chemotherapy or radiation therapy to the head and neck area. 4- Habits as heavy smoking and alcoholism. 5- Patients with T.M.J disorders or poor neuromuscular co-ordination.

  1. For all patient's conventional complete denture will be constructed and adjusted for insertion and delivery.

  2. A cone beam C.T will be done for each patient to determine the bone quality and quantity.

  3. A surgical stent will be designed and fabricated to allow accurate implant placement of two axially placed anterior implants and two distally tilted posterior implants by about 30 degree to support mandibular overdenture.

  4. Surgical placement of implant fixtures on its sites will be done.

  5. Multiunit abutments were screwed to the distal implants.

  6. The conventional mandibular denture will be modified to act as immediate fixed prosthesis that replace lost teeth and gingival tissues.

  7. After three months, the Polyetheretherketone (PEEK) frame that connects the four implants will be constructed using digital scan and CAD CAM manufacturing.

  8. The milled frame was fixed to the metal caps using DTK cement

  9. The BioHPP framework will have prepared abutments projecting from it. After processing, the framework will be tried in patient mouth for passive fit.

  10. Wax interocclusal record was made to establish the occlusal relationship with opposing teeth.

    According to the artificial teeth, the patients will be divided into two groups:

    • Group (I): PEEK framework veneered with nanocomposite resin(visio-lign)
    • Group (II): PEEK framework veneered with zirconia
  11. The inner surface of the artificial teeth will be etched using hydrophosphoric acid then silane will be used and light cured resin cement will be used for cementation of the artificial teeth to the PEEK framework

  12. The occlusal scheme used with the opposing maxillary denture will be lingualized balanced occlusion to enhance the stability of mandibular implant overdentures.

Methods of evaluation:

1- Occlusal force analysis using digital occlusal device (occluscan).

The evaluation periods will be done at time of insertion (T0), 6 month (T1), 12 month (T2) and 18 month (T3) after framework insertion.

Enrollment

30 patients

Sex

Male

Ages

45 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 1- lack of satisfaction of mandibular conventional dentures due to denture instability. 2- Atrophy of mandibular ridges with insufficient bone. 3- They were healthy, free from any systemic diseases relating to bone resorption. 4- All patients have sufficient inter-arch space >15 mm. 5- Maxillary and mandibular residual alveolar ridges covered by healthy non-inflamed mucosa with even compressibility. 6- Normal maxilla-mandibular relationship (class I Angle's classification). 7- All patients will have mandibular bone height not less than 8-10mm as verified by cone beam CT. 8- Sufficient inter-arch space not less than 23 mm as verified by tentative jaw relation. And restorative space not less than14 mm as verified by putty index technique.

Exclusion criteria

  • 1- Systemic disorders affecting bone (such as uncontrolled diabetes mellitus and osteoporosis). 2- Local or general contraindication for surgical procedures. 3- History of chemotherapy or radiation therapy to the head and neck area. 4- Habits as heavy smoking and alcoholism. 5- Patients with T.M.J disorders or poor neuromuscular co-ordination.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

PEEK framework veneered with nanocomposite resin(visio-lign)
Experimental group
Description:
patients recieved 4 implants according to All on 4 concept then peek framework was delivered and veneered with nano-composite resin (visio-lign) as an occlusal material
Treatment:
Procedure: visio-lign nano composite
Procedure: peek framework
Procedure: dental implants
PEEK framework veneered with zirconia crowns
Experimental group
Description:
patients recieved 4 implants according to All on 4 concept then peek framework was delivered and veneered with zirconia crowns as an occlusal material
Treatment:
Procedure: peek framework
Procedure: dental implants
Procedure: zirconia crowns

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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