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OpenTrials
Completed

NCT Number: NCT05972538

Clinical Performance and Stability of Different Types of Implant Supported Overdenture

A Total number of 36 implants were installed in 6 patients having mandibular single denture.

The patients were divided into two groups according to the definitive prosthesis.

Group I received ball and socket retained mandibular implant overdenture while Group II received cement retained implant supported fixed bridges.

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Key information

Conditions

Complete Edentulism Behavior Health Behavior Patient Satisfaction Treatment Adherence and Compliance

Age range

40 year–60 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

National Research Centre

Cairo, Dokki, 12622, Egypt

About this study

Implant's stability, clinical performance (gingival index, pocket depth, plaque index and bleeding on probing) and patient's satisfaction were performed after 15, 30,60 and 90 days after prosthesis delivery

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • highly co-operative
  • non-smoker
  • systemically free from any chronic diseases

Exclusion criteria

  • immunocompromised patients
  • patients having knife edge, flat or flabby ridge,
  • patients having T. M. J disorders

Treatment and study plan

Osstell ( Osstell AB, Goteborg, Sweden).

Device

Implant stability were assessed on 15, 30,60 and 90 days of prosthesis delivery

periodontal probe (Vivacare, TPS, Vivadent, Schaan, Lichtenstein

Device

Clinical evaluation included assessment of pocket depth, plaque index and bleeding on probing) around the implant abutments on 15, 30,60 and 90 days of prosthesis delivery

Other names: - Assessment of implants clinical performance

questionnaire for patient satisfaction

Other

A questionnaire was used to evaluate patient satisfaction on 90 days at the end of follow up period.

Primary outcomes

  1. Assessment of change in implant stability

    Time frame: on the 15th, 30th, 60th and 90th days of overdenture insertion

    Assessment of implant stability by device ( Ostell device)

  2. Assessment of change in implants clinical performance throughout the follow-up period.

    Time frame: on the 15th, 30th, 60th and 90th days of over denture insertion.

    Assessment of change in pocket depth, plaque index and bleeding on probing) around the implant abutments. by periodontal probe.

Secondary outcomes

  1. Assessment of patient satisfaction

    Time frame: on the 90th day of prosthesis delivery

    A questionnaire was used to evaluate patient satisfaction

Sponsors and collaborators

Lead sponsor

National Research Centre, Egypt

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Aug 2, 2023
Registry last updated
Aug 2, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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