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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04990999
Other study ID # vestibular extraction 2021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date February 1, 2021

Study information

Verified date August 2021
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

study proposes an alternative atraumatic tooth extraction procedure; Apically achieved exodontia, which might offer an alternative to the conventional incisal exodontia, whilst providing minimum tissue trauma and subsequently maximum marginal tissue preservation.


Description:

A sample of 26 patients that received the extraction therapy For Group (A) patients, Atraumatic extractions using periotomes followed by conventional forceps were performed. For Group (B) patients, the novel technique of Vestibular Root Extraction was performed to the sample group's hopeless teeth.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date February 1, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Single non-adjacent hopeless maxillary anterior teeth - Type II socket) - Intact overlying soft tissues. - Adequate palatal and at least 3 mm apical bone Exclusion Criteria: - Smokers - Pregnant females - Patients with systemic diseases

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Vestibular Root Extraction
a 1-cm long vestibular access incision was cut, 3-4 mm apical to the mucogingival junction of the involved tooth, then pushing the vestibular pouch in an incisal direction exposing the apical root area, and allowing direct undisturbed access to the root surface
Atraumatic extractions using periotomes followed by conventional forceps
a sulcular releasing incision suing a micro scalpel was made to detach the surrounding tissues, followed by applying the periotome interproximally into the PDL space, widening the attached periodontal ligaments space.

Locations

Country Name City State
Egypt Private Practice Clinic Alexandria

Sponsors (1)

Lead Sponsor Collaborator
Hams Hamed Abdelrahman

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in post restorative soft tissue height identified midfacially and at the apex of the mesial and distal papillae by superimposing the STL (Standard Triangle Language) files of the models, obtained via IOS at baseline and 12 months
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