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Maintenance of Post-Extraction alveolar sockets with Buccal Bone Defect

Maintenance of Post-Extraction Alveolar Sockets with Vestibular Bone Defect

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5944yh
Enrollment
Unknown
Registered
2017-11-24
Start date
2015-03-02
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Loss of Alveolar Bone in post-extraction alveolar sockets with vestibular bone defects

Interventions

Control group: in 10 patients requiring extraction of teeth for posterior implant installation will be performed alveolar preservation with deproteinized bovine bone, collagen membrane and free gingiv
Procedure/surgery
E04.545.562.500

Sponsors

Faculdade de Odontologia de Araraquara-Unesp
Lead Sponsor
Faculdade de Odontologia de Araraquara-Unesp
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Good oral hygiene with plaque index less than 20%; presence of teeth adjacent to the tooth to be extracted with harmonical gingival architecture; age between 18-65 years; clinical attachment level in the vestibular sites > 3 mm.

Exclusion criteria

Exclusion criteria: history of periodontal surgical procedures in the surgical site; Presence of systemic impairment that makes it impossible to carry out the surgeries; presence of infection involving the gingival margin; smokers, bruxism, alcoholics, drug users, diabetics, pregnants, History of radiotherapy in the head and neck region, users of medications that may interfere with the bone remodeling, presence of pathologies that affect bone metabolism.

Design outcomes

Primary

MeasureTime frame
It is expected that both groups will present increased bone volume that will be assessed by CT scans after the 120 day period of the surgical procedure.

Secondary

MeasureTime frame
It is expect that the test group presented less time of surgical procedure and less reports of postoperative discomfort for the patients compared to the control group. The method used for these analyzes will be the application of the VAS scale (first postoperative week) and the surgical time marking.

Countries

Brazil

Contacts

Public ContactElcio Marcantonio Junior

Faculdade de Odontologia de Araraquara-Unesp

elciojr@foar.unesp.br+55(16)33016378

Outcome results

None listed

Source: REBEC (via WHO ICTRP)