Effect of T-scan Occlusal Analysis and Adjustment vs Articulating

Occlusion Clinical Trial

Official title:

Effect of T-scan Occlusal Analysis and Adjustment vs Articulating Paper on Stresses Transmitted to Single Mandibular Implant Supported Prosthesis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05051878
• Other study ID #: OCCLUSAL EVALUATION
• Status: Completed
• Phase: N/A
• Start date: October 1, 2021
• Est. completion date: December 30, 2021

Study information

• Verified date: January 2023
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to compare two different methods for occlusal analysis of implant - supported prosthesis (T-scan and conventional method with articulating papers) regarding the stresses transmitted to the implants.

Description:

Four implants will be inserted, two implants in canine regions and two implants in lower second premolar regions.

After 3 months, two identical overdentures will be constructed for the patient on implants.

The occlusion of each one of the two identical prostheses will be adjusted intraorally but according to different occlusal analysis:

• Group (A) : occlusal adjustments for the overdenture will be done according to articulating paper analysis.

• Group (B) :- occlusal adjustments for the overdenture will be done according to T-scan analysis.

The two prostheses will be retained on dummy implants on acrylic cast and will be loaded under chewing simulator.

The strain developed around the dummy implants will be measured. The data will be recorded manually then will be transferred into digital form. The obtained data will be recorded, tabulated and statistically analyzed using the appropriate tests for comparison within each group.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 7
• Est. completion date: December 30, 2021
• Est. primary completion date: November 30, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 55 Years to 65 Years

Eligibility

Inclusion Criteria:

• Age range from 55-65.

• Radiographic examination should reveal bone height more than 10 mm and crestal bone width not less than 5 mm of the inter-foraminal region.

• Residual bone and mucosa should be free from any pathological signs, bony undercuts, or neoplasia.

• Adequate salivary flow.

• Adequate mouth opening.

• Adequate inter-arch space.

Exclusion Criteria:

• Systemic diseases affecting metabolism of bone e.g uncontrolled diabetes, bone diseases, hyperparathyroidism and renal disease.

• Severe blood diseases (hemophilia etc.).

• Severe vascular heart disease.

• Liver Problems.

• Cerebral infarction .

• Severe immunodeficiency.

• Patients who are undergoing strong chemotherapy.

• Excessive alcohol consumption.

• Severe neuropsychiatric disease, mental disability, and narcotic drug addict

• Uncooperative patients

Related Conditions & MeSH terms

• Occlusion

Intervention

Device:
• T-scan
occlusal analysis T-scan

Other:
• articulating paper
articulating paper occlusal analysis

Locations

Country	Name	City	State
Egypt	Faculty of dentistry, Ain Shams University	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	stresses around implants	stresses transmitted around implants supporting the prosthesis by stain gauge	baseline