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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03287934
Other study ID # R.prosthodontic department
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2017
Est. completion date February 11, 2020

Study information

Verified date July 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

patient with non-restorable tooth in the esthetic zone will be recruited in the study. a traumatic is done and implant will be placed using either digital light processed guides for control group or selective laser sintering group for intervention group.


Description:

the principle investigator will randomize and equally distribute the Eligible patients between the selective laser sintering group (intervention group) and digital light processing group (control group).

- Diagnostic phase : for initial diagnosis, principle investigator will make primary impression , bite registration, face bow record and periapical x-ray for each eligible patients. The tooth to be extracted will be removed from the cast and replaced with an artificial tooth. For construction of radio graphic stent, a clear thermoplastic sheet will be pressed on the modified cast using a vacuum forming machine . A hole is done in the center of the artificial tooth packed with heated gutta percha (radiopaque material) for easy visualization on the cone beam during virtual implant placing. A dual scan protocol with cone beam CT will be made. The first scan is for the patient wearing the scan appliance while the second will be for the cast with the scan appliance.

- Planning phase : placing of the virtual implant and designing of the surgical stent will be done by virtual planning software .

- Construction of the surgical guide: principle investigator will send the Standard Language transformation (STL) file of the designed guide to a rapid prototyping center. Selective laser sintering and digital light procesing will be used for intervention and control group respectively. principle investigator will check for adaption of the guide on the cast and cement the metallic sleeve to prevent rotation during surgery.

- Surgical phase : principle investigator will prescribe a prophylactic antibiotic to the patient three days prior the surgery. Atraumatic extraction will be carried by periotomes and lancet. The integrity of the socket will be examined well by probe. The guide is stabilized in its place then drilling and implant placement will be done. Healing abutment is screwed in place to allow proper healing of the soft tissue. Patient will be instructed to avoid hard foods and follow restrict oral hygiene measures. Patient will be recalled after one week for postoperative inspection and assessment. A cone beam CT will be taken for deviation assessment.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date February 11, 2020
Est. primary completion date January 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Patient age should be more than 18 years old

2. Hopeless tooth in esthetic zone due to caries, endodontical problem or trauma with both neighboring teeth present.

3. Good oral hygiene

4. No periapical lesions (acute accesses or chronic fistula)

5. Adequate bone (5 mm) below the tooth to allow primary implant stability

6. Sufficient Medio-distal bone about 1.5 from each side

7. sufficient labial bone

8. sufficient band of keratinized mucosa

Exclusion Criteria:

1. heavy smoking

2. any systemic condition that is considered absolute contraindication for implant placement

3. pregnancy

4. in adequate inter-arch space

5. parafunctional habits as bruxism

Study Design


Related Conditions & MeSH terms


Intervention

Device:
selective laser sintered stent
after planning and virtual implant placement, a guide will be designed and the STL file will be send to prototyping center for printing the guide with selective laser sintering technique. during the surgical procedure , the target tooth will be atraumatic extracted, the stent is adapted in its place then implant drilling and placement will be done.
digital light processing(dlp)
after planning and virtual implant placement, a guide will be designed and the STL file will be send to prototyping center for printing the guide with digital light processing technique. during the surgical procedure , the target tooth will be atraumatic extracted, the stent is adapted in its place then implant drilling and placement will be done.

Locations

Country Name City State
Egypt Faculty of Dentistry Cairo University Cairo Manil

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Abduo, J., Lyons, K. & Bennamoun, M., 2014. Trends in Computer-Aided Manufacturing in Prosthodontics: A Review of the Available Streams. International Journal of Dentistry, 2014, pp.1-15. Available at: http://www.hindawi.com/journals/ijd/2014/783948/. Alzoubi, Fawaz, Nima Massoomi, and A.N., 2016. Accuracy Assessment of Immediate and Delayed Implant Placements Using CAD/CAM Surgical Guides. Journal of Oral Implantology ., 42(5), pp.391-398. Arisan, V. et al., 2013. Implant Positioning Errors in Freehand and Computer-Aided Placement Methods: A Single-Blind Clinical Comparative Study. The International Journal of Oral & Maxillofacial Implants, 28(1), pp.190-204. Available at: http://www.quintpub.com/journals/find_article.php?doi=10.11607/jomi.2691.

Outcome

Type Measure Description Time frame Safety issue
Primary evaluation of accuracy of implant placement clinical observation measuring both angular and linear deviation of implants by virtual ruler in terms of mm 1 week
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03281148 - Accuracy in Computer Guided Versus Free Hand Immediate Implantation N/A
Active, not recruiting NCT05776498 - Evaluation of Immediate Implant Placement Using Dual Zone Approach Versus Connective Tissue Graft N/A
Completed NCT03243695 - Influence of Abutment Angulation on Implant Failure in Immediately Placed and Restored Implants in the Esthetic Zone Using Computer Aided Surgical Guides: RCT N/A