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Smart Box With OT Equator Attachment in Retaining Implant-assisted Overdenture for the Atrophic Maxilla.

Smart Box Accompanied With OT Equator Attachment in Retaining Immediately Loaded Inclined Implant Assisted Overdenture for Atrophic Maxilla

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05352620
Enrollment
10
Registered
2022-04-29
Start date
2018-03-01
Completion date
2019-05-01
Last updated
2022-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrophic Maxilla, Edentulous Jaw

Brief summary

The aim of the present study is to clinically and radiographically evaluate the effect of the use of recently developed Smart Box accompanied with OT Equator attachment in retaining of the inclined implant assisted overdenture for atrophic maxilla and to compare the vertical bone changes around axial implants with OT Equator attachment and inclined implants with smart box attachment radiographically using CBCT

Interventions

OTHERImplant assisted maxillary overdenture

For each patient, an implant assisted maxillary overdenture will be fabricated using a minimally invasive flapless surgical technique with OT-Equator and Smart Box attachment

Sponsors

Hams Hamed Abdelrahman
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male patients with comparable age (30- 65 years). * All patients should have retruded, posteriorly atrophic completely edentulous maxilla with sinus pneumatization leaving less than 7mm bone height posteriorly and a sufficient amount of bone in the inter bicuspids region. * Opposing mandibular dentate arch including bilateral posterior teeth. * All patients should have an adequate zone of keratinized mucosa. * All patients should be free from any intra-oral or systemic diseases that would otherwise affect the osseointegration of dental implants. * All patients should be well motivated, cooperative, and with adequate manual dexterity necessary to place and remove removable implant prosthesis to provide adequate oral hygiene around the endosseous implants.

Exclusion criteria

* Patients with flabby maxillary ridges. * Patients who are unwilling to accept implant overdentures as a treatment modality. * Patients with temporomandibular and neuromuscular disorders.

Design outcomes

Primary

MeasureTime frameDescription
change in peri-implant probing depthBaseline, 3 months, 6 months, 9 monthsThe peri-implant sulcus depth will be measured using a graduated plastic periodontal probe.
Change in Clinical Attachment levelBaseline, 3 months, 6 months, 9 monthsIt is the distance from the junction implant/abutment to the most apically probable portion, in millimeters
Change in Implant Stabilityat baseline and 9 monthsThe Osstell unit records a numeric value of 1-100 which is referred to as the implant stability quotient (ISQ)
Change in alveolar bone levelat baseline and 9 monthsThe level of alveolar bone around each abutment will be evaluated using CBCT.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026