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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05912127
Other study ID # A09071221
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 16, 2022
Est. completion date June 11, 2023

Study information

Verified date June 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the evaluation of patient satisfaction of All on-4 versus All on-3 implant treatment concepts rehabilitation of atrophied mandibular ridge.


Description:

Patients will be classified into 2 groups according to the implant treatment concept they received: - Group 1 (control group); included patients who received All on 4 implant-supported fixed restoration. The patients received 2 inclined implants anterior to the mental foramina and 2 vertical implants in the lateral incisor/canine areas. - Group 2 (test group); included patients who received All on 3 implant-supported fixed restoration. The patients received 2 inclined implants anterior to the mental foramina and 1 vertical implant in the midline of the mandible.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 11, 2023
Est. primary completion date October 9, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria: - 1. All patients already have implants inserted in their mandibular ridges According to the All on 4 or All on 3 concepts. 2. They were healthy, free from any systemic diseases relating to bone resorption such as uncontrolled diabetes or osteoporosis. This was achieved through medical history and clinical examination by the physician. 3. All patients have sufficient inter-arch space. 4. All patients are of angle class I maxillo-mandibular relationships. 5. All patients had maxillary conventional complete dentures. Exclusion Criteria: 1. Any neuromuscular disorders 2. Uncooperative patients -

Study Design


Related Conditions & MeSH terms


Intervention

Device:
implant supported fixed full arch prosthesis
the patients will receive screw-retained cast metal-ceramic fixed prostheses that replace lost gingival tissues with pink porcelain.

Locations

Country Name City State
Egypt Christine Ibrahim Mansoura

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary patient satisfaction Patient satisfaction was evaluated using a questionnaire based on visual analog scale (VAS) one year
Primary crestal bone loss bone loss was measured around the implants in mm Two year
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