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Stability, Marginal Bone Loss and Occlusal Load Analysis of PEEK Abutment Supported on Short Implant

F

Faculty of Dental Medicine for Girls

Status

Unknown

Conditions

Marginal Bone Loss and Loss of Osteointegration of Short Implant

Treatments

Other: customization of abutment

Study type

Interventional

Funder types

Other

Identifiers

NCT04972240
P-CR-21-03

Details and patient eligibility

About

this study will be directed toward evaluating stability, marginal bone loss and occlusal load of posterior customized PEEK abutments on Ti-bases supported by short implant

Full description

although short implant solved many clinical problems; it is sometimes associated with loss of osseointegration which is firstly expressed by peri-implantitis and marginal bone loss. Also, PEEK is a very promising material characterized by low modulus of elasticity thus it can act as a shock absorber. Whether constructing superstructure components of short implant from PEEK will improve their performance or not is lacking in the dental literature.

To conduct the present study, the following will be used:

  1. Customized screw retained PEEK abutment/crown on a Ti base.
  2. Prefabricated titanium abutment.
  3. Short implant. The study will be conducted on 12 patients with missing single posterior tooth indicated for short implants) near anatomical structure or atrophic ridge), attending the outpatient clinic of the Crowns and Bridges department, Faculty of Dental Medicine for Girls, Al-Azhar University.

Enrollment

12 estimated patients

Sex

All

Ages

30 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

    1. Age range of patients 30-45 years old, with no gender prediction, able to read and sign the informed consent. 2. Patient with missing posterior tooth indicated for replacement with short implant as there are any anatomical limitation (near maxillary sinus or inferior alveolar nerve) or atrophic ridge. 3. Opposing natural teeth should be present. 4. The edentulous ridge should be free from any infection or remining root. 5. Patient should be able to tolerate surgical procedure of implant procedures physically and psychologically. 6. Patient should be willing to return for follow-up examination and evaluation.

Exclusion criteria

    1. Patients with active periodontal diseases. 2. Patient with poor oral hygiene and motivation. 3. Pregnant women. 4. Patient with unrealistic expectations. 5. Patients with parafunctional habits and smoker. 6. Patient with systemic disease and immunocompromised patients which will prevent surgical procedure. 7. Recent extraction or extraction socket with infection or remining root.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

12 participants in 2 patient groups

Customized PEEK abutment/ crown on a Ti base.
Active Comparator group
Treatment:
Other: customization of abutment
Prefabricated titanium abutment, supporting ceramometal separate crown.
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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