NCT03719235

Brief Summary

measurements performed directly on dry mandibles will be compared with measurements obtained from CBCT( ultra-low dose) scans and Digital panoramic radiography.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2018

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

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

Study Start

First participant enrolled

July 10, 2018

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

October 22, 2018

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 25, 2018

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2020

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 10, 2020

Completed
Last Updated

October 25, 2018

Status Verified

October 1, 2018

Enrollment Period

2 years

First QC Date

October 22, 2018

Last Update Submit

October 24, 2018

Conditions

Cone Beam Computed Tomography

Outcome Measures

Primary Outcomes (1)

  • assessment of diagnostic accuracy of linear measurements

    measurements made on dry mandibles will be compared with measurements obtained from CBCT scans \& digital panoramic radiography

    within 2 years

Study Arms (1)

column

OTHER

ultra-low dose CBCT versus digital panoramic radsiography

Other: CBCT

Interventions

CBCTOTHER

ultra-low dose CBCT

column

Eligibility Criteria

Age10 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • age 10 to 70 years
  • no gender nor race predilection
  • Either dentulous or edentulous are acceptable.

You may not qualify if:

  • fractures
  • pathology

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo University

Cairo, 12411, Egypt

RECRUITING

Central Study Contacts

hala wk el fayoumy

CONTACT

01112222565halaelfayoumy@hotmail.com

mohamed md el sawy

CONTACT

01005001650mohamed.mourad@yahoo.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

October 22, 2018

First Posted

October 25, 2018

Study Start

July 10, 2018

Primary Completion

July 10, 2020

Study Completion

September 10, 2020

Last Updated

October 25, 2018

Record last verified: 2018-10

Locations

EG(1)