Status:

COMPLETED

(PEKK) Framework for Mandibular Implant-supported Complete Fixed Prostheses

Lead Sponsor:

Fatma mahanna

Conditions:

Bone Loss

Peri-Implantitis

Eligibility:

All Genders

50-70 years

Phase:

NA

Brief Summary

This clinical study aims to evaluate the effect of using PEKK (Pekkton) framework in mandibular implant-supported complete fixed dental prostheses with All-on-four treatment concept on peri-implant ti...

Detailed Description

The aim of this clinical study is to evaluate the effect of using PEKK (Pekkton) framework in mandibular implant-supported complete fixed dental prostheses with All-on-four treatment concept on peri-i...

Eligibility Criteria

Inclusion

  • Maxillary and mandibular alveolar ridges were covered with healthy, firm, relatively even thickness and even compressible mucosa and free from any signs of inflammation or flabbiness.
  • Patients had completely edentulous maxillary and mandibular ridges with sufficient mandibular bone height not less than 15 mm in the interforaminal area and at least 12mm posteriorly
  • All patients had sufficient inter-arch space
  • All patients complained of insufficient retention and stability of their conventional mandibular dentures.
  • All patients were of Angel's class I maxillo-mandibular relationship.

Exclusion

  • Patients with absolute contraindications for implant placement, such as active cancer and diseases of the immune system.
  • Patients with metabolic diseases that are directly related to bone resorption, such as uncontrolled diabetes, osteoporosis, and hyperparathyroidism.
  • Patients with general contraindications for surgical procedures, such as hematologic diseases, hepatic patients, patients with bleeding disorders, and serious problems with coagulation.
  • Patients with a history of irradiation of the head and neck region or chemotherapy in the last 3 years were also excluded.
  • Patients with relative contraindications such as a history of parafunctional habits (such as bruxism and clenching), smoking, alcoholism, and patients with any physical reasons that could affect follow-up.
  • Patients with local contraindications for implant placement, such as localized bone defects.

Key Trial Info

Start Date :

May 10 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 10 2023

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT06164990

Start Date

May 10 2022

End Date

November 10 2023

Last Update

December 11 2023

Active Locations (1)

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1

Faculty of dentistry, mansoura university

Al Mansurah, Dakahlia Governorate, Egypt, 35511