Status:

UNKNOWN

The Influence of Vertical Implant Position With Immediate Provisionalization on the Marginal Bone Loss.

Lead Sponsor:

Cairo University

Conditions:

Dental Implant Failed

Implant Site Reaction

Eligibility:

All Genders

18-50 years

Phase:

NA

Brief Summary

Multiple clinical studies have established high survival rates and tremendous predictability of dental implant treatment. However, a pleasant esthetic outcome is the patient's primary expectation rega...

Detailed Description

Preservation of crestal bone is crucial and must be prioritized from the onset of implant placement. Adequate amount of peri-implant bone contributes to esthetic success and implant stability. Crestal...

Eligibility Criteria

Inclusion

  • ● Patients with single missing upper anterior or premolar teeth
  • Patients with minimum buccolingual width of 6 mm and mesiodistal width of 6mm
  • Patients with healthy systemic conditions.
  • Patients older than 18 years.
  • Good oral hygiene.
  • Accepts one year follow-up period (cooperative patients).
  • The patient provides informed consent.
  • Adequate Inter-arch space for implant placement.
  • Favorable occlusion (no traumatic occlusion).
  • Absence of allergy to the prescribed medications.

Exclusion

  • ● Patients with inadequate bone volume and/ or quality
  • Patients with local root remnants
  • Patients with inadequate wound healing
  • Patients with signs of acute infection related to the area of interest.
  • Patients with habits that may jeopardize the implant longevity and affect the results of the study such as parafunctional habits (Lobbezoo et al., 2006).
  • Heavy smokers patients (more than 10 cigarettes per day) (Lambert, Morris and Ochi, 2000).
  • Metabolic diseases such as diabetes or hyperthyroidism as well as systemic medications such as chemotherapy or bisphosphonates
  • Pregnant or nursing women.
  • Uncooperative patients.

Key Trial Info

Start Date :

September 20 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 30 2025

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT05973357

Start Date

September 20 2023

End Date

October 30 2025

Last Update

August 2 2023

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