Health TrialsbyHealthPanel

Vibropneumostimulation in the Rehabilitation After Dental Implantation

ConditionDental Implantation
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorSamara State Medical University

About this trial

A new comprehensive technique of dental implantation and rehabilitation of patients will be developed and theoretically justified, including an individual dental implant of a dowel system made of non-woven titanium material with through porosity and vibropneumostimulation, which will improve the functional and anatomical results of treatment.

In the complex treatment and rehabilitation of patients after dental implantation, a vibropneumostimulator with vibratodes of its own design will be used, which activate bone remodeling, which will expand the practical application and theoretical knowledge in the field of hardware massage.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients with a history of previous unsuccessful implantations,

patients with a history of bad habits,

patients with low bone density (CT),

patients who have sinus lifting surgery performed simultaneously

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Vibropneumostimulation

    Device

    New vibrators and techniques of vibropneumostimulation of periimplant tissues have been developed, which will allow us to develop a new concept of the relationship of bone remodulation processes around implants of various designs.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: A group with exposure of vibropneumostimulationExperimental treatment 1 intervention
Group B: A group of standart therapyNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

restoration of dentition by installing crowns on the installed implants

implant stability according to the method of Resonance Frequency Analysis that register magnetic vibrations of the pin together with the implant in the form of an indicator Implant Stability Quotient

Time frame
4 months

Secondary outcomes

1

installation of the gumformer

rate of patients with installation of the gumformer on the installed implants according to the X-ray

Time frame
7 months
2

the beginning of the functional load

rate of patients with the beginning of the functional load on the restored dentition according to the X-ray

Time frame
7 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Samara State Medical University

Lead sponsor

Source ClinicalTrials.gov
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