Soft Tissue Volume Changes in the Posterior Area With Socket Sealing Abutment. Randomized Controlled Trial.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Dental Implants
- Sponsor
- Aula Dental Avanzada
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Soft tissue dimensional changes
- Status
- Active, not recruiting
- Last Updated
- 8 months ago
Overview
Brief Summary
The aim is to clinically evaluate the effect of the alveolar sealing technique using a customised abutment on soft tissue volume changes following molar extraction and immediate dental implant placement.
Detailed Description
A sample of 20 patients in ASAI health status who agree to be involved in the study after giving their consent and who require immediate post-extraction implant treatment in the molar area will be recruited. The soft tissue status before and 6 months after tooth extraction will be recorded by means of a digital impression taken with the same intraoral scanner. The patient will be asked to complete a 7-question questionnaire to inform us about his or her perception of the therapeutic process and the final result. A comparative volume measurement will be made by digitally superimposing the two mesh files obtained before and 6 months after the treatment. Statistical data will be analysed by an external statistician and conclusions will be drawn about the effect of the technique on soft tissue volume as well as the patient's perception of the procedure and its outcome.
Investigators
Guillem Esteve-Pardo
Principal Investigator
Aula Dental Avanzada
Eligibility Criteria
Inclusion Criteria
- •Patients ASA I
- •Need for molar postextraction immediate implant
Exclusion Criteria
- •When the cortical bone is affected and the alveolus presents bone deficiencies
- •When dental implant may not be placed due to medical conditions
Outcomes
Primary Outcomes
Soft tissue dimensional changes
Time Frame: From 0 to 6 months
The changes that occur in the soft tissues in millimetres by comparing the digital impressions before and 6 months after the treatment using specific software.
Secondary Outcomes
- Patients satisfaction(From 0 to 6 months)