Investigation of morphological change (volume increase or decrease) of the soft tissue during the wound healing process after single tooth extraction. /
Conditions
Interventions
Group 1: Control group: conventional tooth extraction using elevator and extraction forceps.
Group 2: Test group: minimally invasive extraction using vertical extractor
Sponsors
Zahnklinik 2 - Zahnärztliche Prothetik
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Obtained informed consent; good general health status; available for the entire 90-day follow-up period; healthy periodontium; at least one tooth in the maxillary anterior region (region 13 to 23) or in the posterior region that can no longer be preserved and can only be treated by extraction
Exclusion criteria
Exclusion criteria: Pregnant and breastfeeding women; Systemic diseases that could affect the outcome of therapy (e.g. uncontrolled diabetes mellitus; current or past radiochemotherapy); Systemic medication that may affect the outcome of therapy (medication that may cause gingival hyperplasia, e.g. anticonvulsants, immunosuppressants, calcium antagonists; antiresorptive therapy, e.g. bisphosphonates or antibodies); existing acute inflammation of the periodontium of the tooth to be extracted (e.g. untreated severe periodontitis; suppuration); Previous mucogingival surgery in the region to be examined (e.g. apicoectomy or aesthetic periodontal rehabilitation)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Completion of the follow-up of the 52nd patient 90 days postoperatively. Continuation of the study and further analyses after one year are planned. There are no criteria for an earlier termination of the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| no secondary endpoint | — |
Countries
Germany
Contacts
Public ContactRagai Edward Matta
Zahnklinik 2 - Zahnärztliche Prothetik
Outcome results
None listed