NCT03164759

Brief Summary

Correlate the implant stability quotient values measured by ostell device with radiographic bone density measured on CBCT by bluesky software pre-operatively

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
35

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2017

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 22, 2017

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 24, 2017

Completed
8 days until next milestone

Study Start

First participant enrolled

June 1, 2017

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2018

Completed
Last Updated

May 24, 2017

Status Verified

May 1, 2017

Enrollment Period

1 year

First QC Date

May 22, 2017

Last Update Submit

May 23, 2017

Conditions

Outcome Measures

Primary Outcomes (2)

  • Bone density

    Measuring bone density on CBCT by bluesky software representing by hounsfield unit pre operatively

    Baseline

  • Implant stability

    Post oprative measurements of implant stability by ostell device (ISQ)

    Immediate post operative

Eligibility Criteria

Age30 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Patients receiving dental implants in healed non grafted sites in both arches

You may qualify if:

  • patients receiving dental implants in both arches
  • patients should be free from any systemic diseases that may affect normal healing of bone, and predicated outcome
  • no intra-oral soft tissue defect that would render primary closure of the intra-oral wound

You may not qualify if:

  • patients with systemic diseases
  • \_ patients with ridge augmentation such as ridge expansion, ridge splitting and bone grafting
  • patients with sinus lifting done to place implants
  • immediate extraction sockets

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Mohammed B Mohammed, Master

CONTACT

Amr H El khadem, Phd

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle investigator

Study Record Dates

First Submitted

May 22, 2017

First Posted

May 24, 2017

Study Start

June 1, 2017

Primary Completion

June 1, 2018

Study Completion

June 1, 2018

Last Updated

May 24, 2017

Record last verified: 2017-05