PEEK Versus Titanium Customized Healing Abutments

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorAin Shams University

About this trial

The study suggests that if the investigators used customized healing abutments synthesized from PEEK may have a favorable effect on peri-implant soft tissues regarding decreased plaque accumulation and healing stimulation compared to the customized conventional titanium healing abutments.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients should be systematically free from any disease as according to Cornell Medical Index-Health Questionnaire .

Both genders.

Age from 20-50 years.

Missing tooth in esthetic zone (Anterior/Premolar) to be restored with standard implant, with no need for additional bone and soft tissue augmentation procedures.

Disqualifiers

Poor oral hygiene condition.

Pregnant and lactating females.

Smokers.

Trial design

Design model

Parallel

Treatments tested in this trial

  • PEEK customized healing abutment

    Device

    Guided delayed implant and a customized PEEK healing abutment placed simultaneously with implant surgery

  • Titanium customized healing abutment

    Device

    Guided delayed implant and a customized Titanium healing abutment placed simultaneously with implant surgery

Treatment groups

26 Participants
are divided into 2 treatment groups
Group A: PEEK customized healing abutment.Experimental treatment 1 intervention
Group B: Titanium customized healing abutment.Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Clinical evaluation of peri-implant soft tissue changes

Clinical evaluation of peri-implant soft tissue changes the Probing Depth (PD).

Time frame
1 month after implantation and 4 months after implantation (just before prosthetic procedures)
2

Clinical evaluation of peri-implant soft tissue changes

Clinical evaluation of peri-implant soft tissue changes the Plaque Index (PI) score.

Time frame
1 month after implantation and 4 months after implantation (just before prosthetic procedures)
3

Clinical evaluation of peri-implant soft tissue changes

Clinical evaluation of peri-implant soft tissue changes the Gingival Index (GI)score.

Time frame
1 month after implantation and 4 months after implantation (just before prosthetic procedures)
4

Clinical evaluation of peri-implant soft tissue changes

Clinical evaluation of peri-implant soft tissue changes the Gingival Bleeding Time Index (GBTI).

Time frame
1 month after implantation and 4 months after implantation (just before prosthetic procedures)

Secondary outcomes

1

Biochemical evaluation

Biochemical evaluation of peri-implant sulcus fluid (PISF) total bacterial load.

Time frame
1 month after implantation and 4 months after implantation (just before prosthetic procedures)

Other outcomes

Sponsors and contacts

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