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Open Sinus ElevationNCT06773637

A Standardized Novel Periapical Radiography Technique for Long Term Follow up of Implants Inserted Simultaneously With Sinus Allogenic Bone Augmentation

An observational study of Open Sinus Elevation and Periapical Radiograph, run by Misr International University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The Aim of this study is introducing a standardized novel periapical radiography technique for long term follow up of implants inserted simultaneously with sinus allogenic bone augmentation. Read more about this study

Who is it for?
Any age
Conditions the study is for
Open Sinus Elevation, Periapical Radiograph
How many people
30 participants
Where
1 siteEgypt
Study dates
1 Jun 2024to 30 Jul 2024
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 Any age
  • All sexes
  • Child, Adult, Older adult

Study population: This novel standardized periapical radiographic technique was introduced and has been performed on patients who were already enrolled in a study performed at Suez Canal University. This aforementioned study was conducted in fulfillment of a PHD thesis that had the ethical approval number of 419/2021. In that study according to its sample size calculation, 30 implants were tested for a long term, 1 year follow up after having undergone open or closed sinus elevation as a surgical procedure (according to the random sequence generated at that time). In addition to simultaneous implant placement and allogenic bone grafting. Hence for the purpose of accurate measurement of mesial and distal marginal bone changes for these implants over the different follow up intervals and up to one year after implant placement a standardized jig had to be created. This jig had to be customized for each patient and had to maintain its shape and integrity and patient position every time a periapical

Who may be able to join

  • 1. Males and females ≥ 18 years of age. 2. ASA I and ASA II. 3. Patients having partial edentulism in the posterior region of the maxilla. 4. Edentulous sites consist of native non augmented bone. 5. Horizontal ridge dimension minimum of 5mm 6. The vertical ridge dimension 4-7 mm. 7. Bone quality of D2 or D3. 8. Enough inter-arch distance. 9. The presence of one-year postoperative radiograph CBCT. 10. Presence of postoperative follow up clinical data.

Who cannot join

  • 1. Patients with active acute infection or residual lesion related to the edentulous sites. 2. Acute maxillary sinus pathosis 3. A remaining root dislodged in the Maxillary sinus. 4. Patients that lack a stable occlusion or have parafunctional habits. 5. Patients with poor oral hygiene who are not amenable to motivation and improvement. 6. Smokers who smoke more than 10 cigarettes a day. 7. Pregnant or lactating mothers. 8. Alcohol and drug abuse. 9. Treatment with radiation therapy in the craniofacial region within the previous 12 months

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Oral & Maxillofacial Surgery Department, Faculty of Dentistry, Suez Canal University

    Ismailia, 41522

Other trials in Egypt

About this study

Official title: Introduction of a Standardized Novel Periapical Radiography Technique for Long Term Follow up of Implants Inserted Simultaneously With Sinus Allogenic Bone Augmentation: A Retrospective Study of a Case Series.

The Aim of this study is introducing a standardized novel periapical radiography technique for long term follow up of implants inserted simultaneously with sinus allogenic bone augmentation.

This novel standardized periapical radiographic technique was introduced and has been performed on patients who were already enrolled in a study performed at Suez Canal University. This aforementioned study was conducted in fulfillment of a PHD thesis that had the ethical approval number of 419/2021.

In that study according to its sample size calculation, 30 implants were tested for a long term, 1 year follow up after having undergone open or closed sinus elevation as a surgical procedure (according to the random sequence generated at that time). In addition to simultaneous implant placement and allogenic bone grafting. Hence for the purpose of accurate measurement of mesial and distal marginal bone changes for these implants over the different follow up intervals and up to one year after implant placement a standardized jig had to be created. This jig had to be customized for each patient and had to maintain its shape and integrity and patient position every time a periapical radiograph was performed. These patients were followed up using this radiographic technique immediate postoperatively, 3, 9 and 12 months postoperatively to evaluate the mesial and distal marginal bone levels according to the previously mentioned study protocol.

Read the detailed description

Introduction and Review of literature The success of dental implants had been for so long identified by variable criteria. (1). However radiographic measurement of marginal bone levels and its loss had always been consistently one of them (2). Intraoral standardized periapical radiography was always the method of choice for such measurement (3).

Paralleling technique is the foundation of an ideal periapical radiograph, since errors in determining the marginal bone height result from any deviation from the proper vertical angle. The use of an aiming and stabilizing device for the film with a silicone bite registration can be very useful for subsequent measurements and comparisons of marginal bone losses (4). However, it has been noted that the visual interpretation of intraoral radiographs has limited diagnostic relevance for the early detection of small changes in bone. That is due to the fact that before alterations in conventional radiographs become visible, roughly 30 to 50% of bone mineral must be lost (5).

Therefore, various techniques for evaluating alveolar bone height have been widely applied in periodontal and implant research. Direct measurements using graded rulers with millimeters or more complex techniques using computer software and digital imagery had been used widely in the literature. While the digital softwares available for evaluation of marginal bone levels have been proven to be very efficient and accurate to use (6).

The use of the DIGORA for Windows (DFW) software was proposed in the literature frequently associated with accurate measurements of marginal bone levels around dental implants. As well as for its significance of density measurements. (7). For many years now, digital radiography has been proved as an accurate tool in detecting small changes in bone density. Consequently, it was found to be suitable for assessing bone healing (8).

It offers several advantages over conventional films mainly is that digital radiographs offer 80 % reduction in radiation doses, time saving, the elimination of dark room procedures, real-time image display, and opportunities for tele-consultations with radiologists are well known to be cost-effective and reliable. The main advantage of digital techniques that is not shared by conventional radiography is that images are not static, but may be, manipulated by image processing to enhance diagnosis (9).

In the studies of maxillary sinus floor elevation with dental implants placement the use of digitally performed standardized periapical radiographs to measure the marginal bone levels gain or loss had been documented in the literature (10).

And in these studies, and other studies using the modality of intra-oral standardized radiography for assessment of marginal bone levels around placed dental implants, the accepted protocol for measurements follow up was usually based on a 3-month analysis such as immediately postoperative, 3 months and 6 months. (11).

Aim of the study The Aim of this study is introducing a standardized novel periapical radiography technique for long term follow up of implants inserted simultaneously with sinus allogenic bone augmentation.

Materials and Methods

Study Population:

This novel standardized periapical radiographic technique was introduced and has been performed on patients who were already enrolled in a study performed at Suez Canal University. This aforementioned study was conducted in fulfillment of a PHD thesis that had the ethical approval number of 419/2021.

In that study according to its sample size calculation, 30 implants were tested for a long term, 1 year follow up after having undergone open or closed sinus elevation as a surgical procedure (according to the random sequence generated at that time). In addition to simultaneous implant placement and allogenic bone grafting. Hence for the purpose of accurate measurement of mesial and distal marginal bone changes for these implants over the different follow up intervals and up to one year after implant placement a standardized jig had to be created. This jig had to be customized for each patient and had to maintain its shape and integrity and patient position every time a periapical radiograph was performed. These patients were followed up using this radiographic technique immediate postoperatively, 3, 9 and 12 months postoperatively to evaluate the mesial and distal marginal bone levels according to the previously mentioned study protocol.

Preparation of the radiographic bite jig for standardized periapical radiographs Mesial and distal marginal bone levels were measured using a standardized periapical software using the the KaVo Scan eXam OneTM intraoral digital imaging photostimulable phosphor (PSP) plate system which is a film-like thin, flexible, and wireless phosphorescent plate and works as a wireless receptor. This plate will be held by a paralleling device suitable to act as a film holder for it which is the extension cone paralleling (XCP) device namely the Rinn XCP-PSP Fit® to facilitate long cone paralleling techniques. However, to standardize the images measurements a radiographic occlusal bite jig was constructed preoperatively and saved for all following visits in accordance with those constructed in the literature for this purpose (12,13).

However, we used in our study rubber base impression material namely ZetaplusTM (condensation silicone elastomeric material) instead of the wax proposed by (12) to ensure its stability for all the following follow up visits.

Outcomes assessment:

Mesial and Distal Marginal bone level:

Marginal bone level was measured at T1, T2, T3 and T4 follow up periods, by using a standardized periapical radiograph using paralleling device film holders and a customized occlusal jig to hold a PSP digital x ray film as was explained before.

The mesial and distal marginal bone levels were recorded at each of the follow up periods by measuring the length on the CLINIVIEWTM software between the implant platform and the highest visible bone level at the mesial and distal levels of the implant.

Statistical analysis

Experimental design and data analysis:

All collected data will be calculated, tabulated, and statistically analyzed using suitable statistical tests as follows.

  1. A normality test will be done to check normal distribution for data by Shapiro-Wilk test.
  2. Descriptive statistics will be calculated in the form of Mean ± Standard deviation (SD), range (Max- Min). Qualitative data will be presented as frequencies (n) and percentages (%).
  3. ANOVA - test or Kruskal-Wallis test (According to the types of data) One-way ANOVA (Analysis of variance) will be used to compare between time interval (more than two intervals). Tukey post-hoc test or other post hoc tests will be performed for the evaluation of statistical significances among the groups.
  4. T- test or Mann-Whitney test (According to the types of data) Independent Student's T-test or Mann-Whitney will be performed for the mean differences between the two groups for normally distributed and not normally distributed respectively.
  5. P<0.05 is considered significant.
  6. Statistical analysis will be performed using the computer program SPSS software for windows version 26.0 (Statistical Package for Social Science, Armonk, NY: IBM Corp)
Keywords
periapical radiograph, dental implants, open sinus elevation, closed sinus elevation

What is being measured

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

  1. Mesial and Distal Marginal bone level:

    Marginal bone level was measured at T1, T2, T3 and T4 follow up periods, by using a standardized periapical radiograph using paralleling device film holders and a customized occlusal jig to hold a PSP digital x ray film as was explained before.

    The mesial and distal marginal bone levels were recorded at each of the follow up periods by measuring the length on the CLINIVIEWTM software between the implant platform and the highest visible bone level at the mesial and distal levels of the implant.

    Measured: 1 year

Timeline

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

  1. First posted14 Jan 2025
  2. Study start1 Jun 2024
  3. Primary completion1 Jul 2024
  4. Study completion30 Jul 2024

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
Cohort
Time perspective
Retrospective
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06773637
Sponsor's protocol ID
2024/842
Status last verified
Jan 2025
First submitted
8 Jan 2025
Last updated
14 Jan 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Open Sinus Elevation and Periapical Radiograph, run by Misr International University at 1 site in Egypt.

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 1 inclusion and 1 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: finished, as of the sponsor's last update on 14 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Mesial and Distal Marginal bone level: (time frame: 1 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 14 Jan 2025.

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