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Apical Gap Length and Adaptation of Zirconia Post Using Intraoral and Extraoral Scan of Silicon Impression Technique

Evaluation of Apical Gap Length and Adaptation of Custom Made Zirconia Post Using Digital Intraoral and Extraoral Scan of Conventional Silicon Impression Technique. (Randomized Controlled Clinical Trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05476419
Enrollment
11
Registered
2022-07-27
Start date
2023-09-30
Completion date
2024-12-31
Last updated
2023-02-09

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

Conditions

Endodontically Treated Teeth

Brief summary

First, participants will undergo clinical and radiographic examination for taking all the needed preoperative records, then endodontically treated teeth preparation starting with removal of any carious or undermined tooth structure then ferrule preparation then followed by intra-radicular preparation and then placement of the provisional restoration. In the third visit we will take the final impression of the post space for each patient by using the intraoral scan and extraoral scan o f the conventional impression. Then assessment of the apical gap length by using digital periapical radiograph using the paralleling technique and assessment of post adaptation using replica technique followed by placement and permanent cementation of the zirconia custom made post and core restoration that showed less apical gap length and better adaptation then taking the final impression for the extracoronal restoration and finally permanent cementation of the extra coronal fixed restoration.

Detailed description

Examination and diagnosis:Selection and examination of the patients according to inclusion and exclusion criteria. Diagnosis of the patient's chief complaint and teeth that will be involved in this study will be done. Primary impression will be taken to produce study cast. The patients will be asked to maintain good oral hygiene measures by using tooth brush twice daily. Taking a professional pre-operative photo. Tooth preparation procedure: 1. Removal of any carious or undermined tooth structure then coronal preparation will be done with a ferrule of at least 1.5 to 2 mm then followed by root canal preparation to an adequate length and diameter. 2. After tooth preparation, the final impression will be taken for the post space for each participant by using the intraoral scan and extraoral scan of the conventional silicone impression. 3. Fabrication of temporary restoration using composite resin temporary material and cemented using Zinc Oxide eugenol free temporary cement. Fabrication of restoration: Monolithic zirconia will be used for the fabrication of post and core restoration. Assessment of the apical gap length by using digital periapical radiograph using the paralleling technique. Assessment of post adaptation using replica technique followed by placement and permanent cementation of the zirconia custom made post and core restoration that showed less apical gap length and better adaptation. Taking the final impression for the extracoronal restoration. Finally permanent cementation of the extra coronal fixed restoration.

Interventions

OTHERDirect intra-oral scanning technique for the post space.

scanning of prepared dental post space directly inside the patient mouth by using an intra-oral scanner

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
16 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age 16-65 years with endodontically treated anterior tooth or teeth & in need of custom made post and core restoration. 2. Be physically and psychologically able to tolerate conventional restorative procedures. 3. Subject tooth free of clinical symptoms & No requirement for endodontic retreatment expressed by the presence of periapical radiolucency around an endodontically treated tooth. 4. Adequate level of oral hygiene expressed by the absence of signs of periodontal inflammation, bleeding on probing and periodontal pocket depth \<4 mm. 5. Capable of signing an informed consent

Exclusion criteria

1. Advanced periodontitis affecting the mobility of the teeth (mobility grade II or higher) 2. Pregnant or lactating females. 3. Patients with Psychiatric problems or unrealistic expectations. 4- Patients with endodontically treated teeth which is not functioning or showing any signs or symptoms that need endodontic retreatment. 5- Occlusion problems. 6- Absence of posterior stopper. \-

Design outcomes

Primary

MeasureTime frameDescription
Apical gap lengththrough study completion, an average of 1 year.measuring apical gap length by the digital Periapical radiograph using the paralleling technique.

Secondary

MeasureTime frameDescription
Post adaptationthrough study completion, an average of 1 year.Measuring post adaptation by using Replica technique

Contacts

Primary ContactRv Mh El-boghdady, Ass lecturer
rivan.elboghdady@dentistry.cu.edu.eg01007172887
Backup ContactRi Ma El-boghdady, Ass lecturer
pinkparadise20@yahoo.com01007172887

Outcome results

None listed

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