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Clinical Trials in Egypt / NCT07250503
Active, not recruiting Not applicable

Compare the Difference in Occlusal Force Distribution and Denture Retention Using 2 Different Denture Base Materials in Implant Retained Overdenture

NCT07250503 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2024-09-01
Last updated
2025-11-26

Condition(s) studied

Edentulous Alveolar Ridge In MandibleComplete EdentulismDental ImplantAttachmentsImplant Retained OverdentureEdentulous Mouth

Investigational drug(s) / intervention(s)

Conventional acrylic resin dentureFlexible resin denture

Conventional acrylic resin denture: Mandibular complete dentures made of heat-cured acrylic resin (PMMA). In the mandible, two implants were inserted in the symphyseal area and retained by Equator attachments.

Flexible resin denture: Mandibular overdentures were made of the flexible acrylic resin breflex, In the mandible, two implants were inserted in the symphyseal area and retained by Equator attachments

Study summary

The global increase in the aging population has led to a rise in total edentulism, which remains a major public health concern. two-implant-retained mandibular overdentures have been regarded as the standard of care, offering superior retention, stability, comfort, and masticatory efficiency compared to conventional dentures. Among available attachment systems-bar, ball, stud, and magnet-the Equator attachment has gained popularity due to its low vertical profile, suitability for limited inter-occlusal space, and ease of handling.

Assessment of masticatory performance and occlusal balance can be objectively measured using devices such as bite force analyzers and the computerized T-Scan system, which quantifies occlusion and disocclusion times.

Conventional heat-cured polymethyl methacrylate (PMMA) remains the most widely used denture base material; however, it has mechanical and biological limitations. Flexible denture base materials have been introduced to overcome these drawbacks by enhancing adaptation, distributing occlusal loads more evenly, and improving comfort and retention.

Eligibility

Sex
ALL
Min age
60 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. All patients age must range from 60-70 years old. 2. All patients' ridges should be covered with firm mucosa free from any signs of inflammation or ulceration and exhibit adequate height and width of the residual alveolar ridge. 3. Patients should be free from any metabolic or bone disorder that contraindicate implant installation. 4. All patients must have sufficient inter arch space Exclusion Criteria: 1. Patients with oral or systemic diseases. 2. Patients with xerostomia or excessive salivation. 3. Patients with parafunctional habits (bruxism or clenching). 4. Heavy smoker or alcoholic patients. 5. Patients with history of temporo-mandibular dysfunction. 6. Patients with brain disorders or psychiatric disorders

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cairo University Cairo Egypt

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07250503 on ClinicalTrials.gov ↗ ← All trials in Egypt