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Compares treatment options for Biting Forces
Official title Evaluation Of Marginal Bone Height Changes And Biting Force In Screw Retained Implant Prostheses Using Reinforced Resin Vs Monolithic Zirconium
ClinicalTrials.gov ID: NCT07007572
What this study is testing
What is Digitally-fabricated implant supported supra-structure fabricated from reinforced resin?
Digitally-fabricated implant supported supra-structure fabricated from reinforced resin is an investigational medicine, being studied as a potential treatment for biting forces.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This studies aims to compare the behavior of recently introduced resin reinforces compared to monolithic zirconia
- Phase 2: a mid-size study of how well it works
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 30 to 60. Healthy volunteers may be eligible.
You may be able to join if
- Mandibular Class II, partially edentulous patients that enables measuring the marginal bone height changes and values of biting forces intra-orally.
- Fully dentulous edentulous opposing Maxillary arch.
- Patients with normal class I jaw relationship.
- Patients that require fixed restorations for functional and esthetic reasons
- Age range (30-60 years).
You likely can't join if
- Patients with Parkinson's disease
- Patients with xerostomia.
- Patients with a history of allergy to resins and/ or zirconia.
- Patients with a medical systematic condition that contraindicate implant placement.
- Patients smoking more than 10 cigarettes per day.
- Patients with pathological changes of residual ridges as recurrent or persistent ulcers, osteomyelitis and infections.
See the full eligibility criteria
- Mandibular Class II, partially edentulous patients that enables measuring the marginal bone height changes and values of biting forces intra-orally.
- Fully dentulous edentulous opposing Maxillary arch.
- Patients with normal class I jaw relationship.
- Patients that require fixed restorations for functional and esthetic reasons
- Age range (30-60 years).
- Cooperative patients those are willing to attend all follow-up periods.
- Patients with healthy attached mucosa of appropriate thickness free from any inflammation.
- Patients with healthy bone of appropriate thickness, width and height free from any inflammation.
- Patients without any medical conditions that contraindicates implant placement.
- Patients with Parkinson's disease
- Patients with xerostomia.
- Patients with a history of allergy to resins and/ or zirconia.
- Patients with a medical systematic condition that contraindicate implant placement.
- Patients smoking more than 10 cigarettes per day.
- Patients with pathological changes of residual ridges as recurrent or persistent ulcers, osteomyelitis and infections.
- Patients with large irregular bony exostosis.
- Patients with medical or psychological conditions as physical disability or mental retardation that hinder cooperation in the follow up visits and answering the questionnaires.
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Cairo Governorate, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 30 years to 60 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Cairo Governorate, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.