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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05112796
Other study ID # VST_PET_20
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date March 24, 2021

Study information

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

Clinical Trial Summary

The current randomized clinical trial aimed to compare the VST versus Partial Extraction Therapy (PET) for immediate implant placement in the esthetic zone in class I fresh extraction sites. The primary outcome was the assessment of vertical dimensional changes in peri-implant soft tissue margin. The secondary outcome was the assessment of radiographic changes in the thickness of the facial peri-implant tissues.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date March 24, 2021
Est. primary completion date March 24, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - single hopeless maxillary tooth in the esthetic zone - non-smokers - systemically healthy - Class I extraction sites Exclusion Criteria: - smoking - Class II and III extraction sites - hopeless teeth with acute infection or vertical/horizontal root fracture

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Class I extractions sites received immediate implants using the Vestibular Socket Therapy
A 1-cm-long vestibular access incision was made using a 15c blade 3 to 4 mm apical to the mucogingival junction at the related socket. A subperiosteal tunnel was created connecting the socket orifice and the vestibular access incision
class I extractions sites received immediate implants using the Partial Extraction Therapy
the hopeless tooth was decoronated 1 mm coronal to the gingival margin using a diamond bur. Then, the facial root segment was separated from the rest of the root using a Lindemann bur in gentle mesiodistal sweeping strokes from the gingival margin to the apex of the root, aiming to separate the palatal and the labial root segments.

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 the peri-implant facial tissue thickness through CBCT images (Carestream 8000D- Carestream Dental) that were taken at baseline and 6 months postoperatively at baseline and 6 months
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