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Clinical Trials in Egypt / NCT07208812
Recruiting Not applicable

3D-Printed Implant Overdentures: Comparing Impression Techniques

NCT07208812 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-01-06
Last updated
2026-01-29

Condition(s) studied

Edentulism

Investigational drug(s) / intervention(s)

Conventional open -tray impressionFunctionally generated reline impressionMucostatic base with functional borders impression

Conventional open -tray impression: Primary impression with irreversible hydrocolloid, custom tray with open window, and final impression with silicone material around impression copings to fabricate a 3D-printed implant overdenture

Functionally generated reline impression: Interim prosthesis relieved and reline impression taken during centric closure with border molding, scanned to construct a 3D-printed implant overdenture

Mucostatic base with functional borders impression: Intraoral scan of edentulous arch, 3D-printed baseplates for occlusion rim, functional border molding, and digital workflow to fabricate 3D-printed implant overdenture

Study summary

This randomized crossover clinical trial aims to compare three different impression techniques for the construction of 3d-printed mandibular implant overdentures in completely edentulous patients. Sixteen patients will receive two mandibular implants and three overdentures fabricated using:(1) conventional open-tray implant level impression (2) functionally generated reline impression, and (3)mucostatic base with functional borders impression. Each overdenture will be worn for three months with a washout period between interventions.

The primary outcome is masticatory efficiency, assessed using a color -mixing ability test at 3,6, and9 months.

Secondary outcome is patient satisfaction, assessed using a Visual Analog Scale (VAS) at the same intervals. the study hypothesis is that the impression technique influences both chewing efficiency and patient satisfaction

Eligibility

Sex
ALL
Min age
45 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy patients, free from systemic diseases that affect bone resorption (e.g., uncontrolled diabetes, osteoporosis) * Residual alveolar ridges covered with healthy, firm mucosa * Adequate mandibular bone length and width to accommodate standard implant sizes. * Angle's Class I maxillo-mandibular relationship. Exclusion Criteria: * Absolute contraindications to implant placement (e.g., active cancer, immune system diseases) * History of head and neck irradiation or chemotherapy within the past 3 years * Metabolic bone diseases such as uncontrolled diabetes, osteoporosis, or hyperparathyroidism * Parafunctional habits such as bruxism or clenching * Smoking or alcoholism * Any physical or medical condition that may interfere with study follow-up or implant success

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry, Mansoura University Al Mansurah Dakahlia Governorate Recruiting

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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 NCT07208812 on ClinicalTrials.gov ↗ ← All trials in Egypt