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Greater Palatine ForamenNCT04970186

Assessment of Anatomical Variations of Greater Palatine Foramen in a Sample of Egyptian Population (CBCT)

An observational study of Greater Palatine Foramen, run by Cairo University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

A cross-sectional study to assess the anatomical variations of greater palatine foramen in a sample of Egyptian population using cone beam computed tomography through retrospective data analysis Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Greater Palatine Foramen
How many people
173 participants
Where
No sites listed yet
Study dates
Aug 2021to Mar 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • Adult, Older adult

Study population: Egyptian Population

Who may be able to join

  • CBCT scans of Adult Egyptian population older than 18 years.
  • CBCT scans showing the floor of the maxillary sinus.
  • No artifacts in the maxillary region, which will affect the quality of the image

Who cannot join

  • CBCT sans of completely edentulous maxilla.
  • Patients with trauma, craniofacial surgery, orthognathic surgery and malignancies involving the maxillofacial region.
  • Patients with cleft palate and other craniofacial anomalies.
  • Dental implants in the alveolar region of premolars and molars due to artifacts.

About this study

Official title: Assessment of Anatomical Variations of Greater Palatine Foramen in a Sample of Egyptian Population Using CBCT: A Hospital-based Cross-Sectional Study

A cross-sectional study to assess the anatomical variations of greater palatine foramen in a sample of Egyptian population using cone beam computed tomography through retrospective data analysis

Read the detailed description
  1. Setting and location:
  2. The CBCT Scans of this study will be obtained from the data base available at the department of Oral and Maxillofacial Radiology, Faculty of Dentistry, Cairo University, Cairo, Egypt.
  3. Being a retrospective study, CBCT scans of Egyptian patients who have already been subjected to CBCT examination as part of their dental diagnosis and/or treatment planning will be included according to the proposed eligibility criteria.

B)Participants:

Based on sample size calculation, a sample of 173 hemi-palate belonging to Egyptian individuals will be examined.

  1. Variables:
  • Details about variable
  1. Diameter of GPF.
  2. Location of GPF in relation to maxillary molars.
  3. The distance between the GPF and the midline maxillary suture (MMS).
  4. The distance between the GPF and the posterior border of the hard palate (PB).
  5. Number of foramina.
  6. Type of the hard palate and relation to GPF location:
  • Palatal index
  • Palatal height index

D)Data sources/ Measurements:

  • Retrospective Data collection will be performed after the CBCT scans are pooled from the computer database.
  • All the CBCT examinations will be scanned using CBCT machine (Planmeca promax 3D Mid).
  • CBCT scans using different fields of view, with 0.4mm voxel size.
  • The following parameters will be measured on these images in sagittal, coronal and axial planes:
  1. Diameter of GPF.
  2. Location of GPF in relation to maxillary molars as described by Ajmani (1994). Between the upper first and second molar - A In the midline of the upper second molar - B Between the upper second and third molar - C In the midline of the upper third molar - D Distal to the upper third molar - E
  3. The distance between the GPF and the midline maxillary suture
  4. The distance between the GPF and the posterior border of the hard palate (PB).
  5. Number of GPF.
  6. Type of the hard palate and relation to GPF location:
  • Palatal index
  • Palatal height index
  • CBCT scans will be interpreted by two oral radiologists independently; blinded from demographic data of the patients and from the results of each other.
  • One of them will evaluate the images twice with a period of two weeks between the two reading sessions.
  • Then inter-observational and intra-observational reliability between the observers will be evaluated.
  1. Addressing potential sources of bias:

No source of bias. CBCT scans will be coded and interpreted by two oral and maxillofacial radiologists independently blinded from demographic data of the patients and from the results of each other.

  1. Study Size:

The aim of the study is to assess the diameter and location of the greater palatine foramen in a sample of Egyptian population. Based upon the results of Ikuta, Carla Renata Sanomiya, et al 2013, the diameter of greater palatine foramen= 3.1 mm (±0.47). Acceptable margin of error=7%, a total sample size of 173 hemi-palate will be sufficient. Sample size calculation was performed using Benchmark Six Sigma.

  1. Sampling strategy: The sample will be collected by convenience sampling.
  2. Quantitative variables:

Subgrouping will be created to assess the variables regarding the gender and side.

  1. Diameter of GPF.
  2. Location of GPF in relation to maxillary molars.
  3. The distance between the GPF and the midline maxillary suture (MMS).
  4. The distance between the GPF and the posterior border of the hard palate (PB).
  5. Number of foramina.
  6. Type of the hard palate and relation to GPF location:
  • Palatal index
  • Palatal height index
  1. Statistical methods:

Data will be analyzed using IBM SPSS advanced statistics (Statistical Package for Social Sciences), version 21 (SPSS Inc., Chicago, IL). Numerical data will be described as mean and standard deviation or median and range. Categorical data will be described as numbers and percentages.

Keywords
Greater palatine foramen, GPF, CBCT, Cone beam computed tomography, Hard palate

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diameter of GPF

    Measuring device is CBCT Software on Planmeca Promax 3D Mid, Measuring unit is mm

    Measured: one year

Secondary outcomes (1)
  1. Location of GPF in relation to maxillary molars.

    Measuring device is CBCT Software on Planmeca Promax 3D Mid, Measuring unit is percentage %

    Measured: one year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jul 2021
  2. Study startAug 2021 (estimated)
  3. Primary completionJan 2022 (estimated)
  4. Study completionMar 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Retrospective
Enrolment
173 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04970186
Sponsor's protocol ID
ORAD 7-1-1
Status last verified
Jul 2021
First submitted
11 Jul 2021
Last updated
21 Jul 2021
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Greater Palatine Foramen, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 21 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diameter of GPF (time frame: one year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2021.

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