Accuracy of Selective Laser Sintered Computer Guided Stents Versus Digital Light Processing Stents in Immediate Implant Placement in Esthetic Zone, a Randomized Controlled Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Cairo University
- Enrollment
- 22
- Locations
- 1
- Primary Endpoint
- evaluation of accuracy of implant placement clinical observation
Study Overview
Brief 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.
Detailed 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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Masking Description
due to the nature of study only the participants could be blinded
Eligibility Criteria
- Ages
- 18 Years to 50 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Patient age should be more than 18 years old
- •Hopeless tooth in esthetic zone due to caries, endodontical problem or trauma with both neighboring teeth present.
- •Good oral hygiene
- •No periapical lesions (acute accesses or chronic fistula)
- •Adequate bone (5 mm) below the tooth to allow primary implant stability
- •Sufficient Medio-distal bone about 1.5 from each side
- •sufficient labial bone
- •sufficient band of keratinized mucosa
Exclusion Criteria
- •heavy smoking
- •any systemic condition that is considered absolute contraindication for implant placement
- •in adequate inter-arch space
- •parafunctional habits as bruxism
Arms & Interventions
digital light processing stent
according to the allocation, the experimental group will receive a digital light processing stent for immediate implant drilling and placement after atraumatic extraction of the target tooth.
Intervention: selective laser sintered stent (Device)
digital light processing stent
according to the allocation, the experimental group will receive a digital light processing stent for immediate implant drilling and placement after atraumatic extraction of the target tooth.
Intervention: digital light processing(dlp) (Device)
selective laser sintering
according to the allocation, the intervention for the control group will be a selective laser sintering stent after atraumatic extraction of the target tooth for immediately implant placement. the selective laser sintering stent will be adapted and drilling will be done through the stent.
Intervention: selective laser sintered stent (Device)
selective laser sintering
according to the allocation, the intervention for the control group will be a selective laser sintering stent after atraumatic extraction of the target tooth for immediately implant placement. the selective laser sintering stent will be adapted and drilling will be done through the stent.
Intervention: digital light processing(dlp) (Device)
Outcomes
Primary Outcomes
evaluation of accuracy of implant placement clinical observation
Time Frame: 1 week
measuring both angular and linear deviation of implants by virtual ruler in terms of mm
Secondary Outcomes
No secondary outcomes reported
Investigators
mahetab hamdi
principal investigator
Cairo University