Evaluation the patient satisfaction and dimensional stability of upper removable partial
denture constructed from two different flexible thermoplastic materials.(BRE-FLEX and PEEK).
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Full eligibility criteria for NCT03025555
Ages eligible for Study
45 Years to 55 Years
Genders eligible for Study
Accepts Healthy Volunteers
All patients must have Kennedy class III modification I upper partially edentulous ridges.
The remaining teeth have good periodontal condition, with no signs of attrition or gingival recession.
Male or female patient with age range (45-55) and in good medical condition
All patients have skeletal Angle's class I maxillo-mandibular relationship and have sufficient interarch distance.
Free from any systemic or neuromuscular disorder that might affect chewing efficiency of masticatory muscles.
Free from any tempro-mandibular joint disorder.
The patients have good oral hygiene and low caries index.
Patients having abnormal habits as bruxism or clenching
Patients having hormonal disorders as diabetes, thyroid or parathyroid hormonal diseases were not included.
Teeth with compromised bone support.
Patient with xerostomia or excessive salivation.
Patient with abnormal tongue behavior and/or size.
All locations for NCT03025555
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Tris trial is registered with FDA with number: NCT03025555. The sponsor of the trial is Cairo University and it is looking for 12 volunteers for the current phase.
Official trial title: COMPARISON OF PATIENT SATISFACTION AND DIMENSIONAL ACCURACY OF INJECTION MOLDED PEEK AND BRE-FLEX MATERIALS FOR BOUNDED REMOVABLE PARTIAL DENTURES (Randomized Clinical Trial)
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