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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06114069
Other study ID # M07100522
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 10, 2022
Est. completion date July 2024

Study information

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

Clinical Trial Summary

the aim of the study to compare the anterior maxillary bone index changes for patient rehabilitated with implant supported fixed prosthesis opposed by natural teeth


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 8
Est. completion date July 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria: - 1. All patient wearing a maxillary implant supported overdenture or implant supported fixed restoration and mandibular natural teeth or fixed restoration within natural dentition. 2. All patients were unsatisfied by the maxillary restoration and presented clear preference for a better prosthesis. 3. They were healthy, free from any systemic diseases relating to bone resorption such as uncontrolled diabetics or osteoporosis. This was achieved through medical history and clinical examination by physician. 4. At least one year passed after the last restoration. 5. At least 15 mm restorative space must be available (from the mucosa covering the crest of the residual ridge to proposed occlusal plane) to permit construction of all types of tested prosthesis (class I according to Ahuja and Cagna).195 This was detected by a tentative jaw relation. Exclusion Criteria: - 1. Patients had head and neck radiotherapy, patients with bleeding disorders or hepatic patients. 2. Patients with metabolic disorders as diabetes mellitus, osteoporosis and hepatic disorders which might affect implant lifespan. 3. Long term immunosuppress and corticosteroid drug therapy. 4. Patient with abnormal habits as clenching and bruxism. 5. Smoking patient. 6. Uncooperative patients. 7. Neuromuscular diseases. 8. Patient with problems in TMJ.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
implant supported maxillary fixed prosthesis
Maxillary fixed prosthesis according to all on four or all on six concept

Locations

Country Name City State
Egypt Amr Saeed Mansoura DK

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary anterior area index outcome is being evaluated by radiograph six months
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