Influence of Acetal Resin Versus Nylon Elastic Cap on Crestal Bone Loss in Mandibular Implant-Supported Overdenture

ConditionsBone Loss Pocket, Periodontal

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexMale

Age40-60

SponsorFuture University in Egypt

About this trial

Objective: To evaluate and compare the effect of two different attachment housing materials-Acetal Resin (Polyoxymethylene) versus conventional Nylon elastic caps-on marginal crestal bone loss around dental implants supporting a mandibular overdenture. It also evaluates peri-implant clinical tissue health by measuring pocket depth and the gingival bleeding index.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Completely edentulous mandible.

Sufficient bone height/width in mandibular residual ridges.

Angles classification class I.

Sufficient inter-arch distance

Disqualifiers

TMJ disorders.

Diabetic

Hypertensive

Cancer patients.

Trial design

Design model

Parallel

Treatments tested in this trial

Acetal Resin
Device
overdenture supported by implants
nylon
Device
overdenture supported by implants

Treatment groups

22 Participants

are divided into 2 treatment groups

Group A: interventionExperimental treatment 1 intervention

Group B: controlActive comparator 1 intervention

Trial outcomes

Primary outcomes

Change in crestal bone levels

Time frame

one year

Secondary outcomes

pocket depth changes

Time frame

one year

Locations

This trial has no locations.

Sponsors and contacts

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

Future University in Egypt

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: