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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03670979
Other study ID # 839/2757
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 5, 2016
Est. completion date January 5, 2017

Study information

Verified date February 2023
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was designed to investigate the use of minimally invasive Piezo knife to harvest vascularized interceptal bone pedicle in treating intrabony defects.


Description:

Sixteen non-smoking patients with severe chronic periodontitis participated in this prospective, randomized clinical study. Patients were randomly assigned into one of a 2 groups (8 patients each): bone substitute grafting of the intrabony defect, control group (Gr1), intrabony defect osseous wall swaging (OWS) combined xenograft (Gr2). In both groups root surfaces where treated with a neutral 24% EDTA gel and saline irrigation. Clinical and radiographic measurements were reassessed at 6 months after surgery.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date January 5, 2017
Est. primary completion date January 5, 2017
Accepts healthy volunteers No
Gender All
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria: 1. good compliance with plaque control instructions following initial therapy 2. teeth involved were all vital with no mobility ; 3. each subject contributed a single predominately 2 or 3-wall intrabony interproximal defect around premolar or molar teeth without furcation involvement; Exclusion Criteria: 1. no systemic diseases which could influence the outcome of therapy; 2. absence of periodontal treatment during the previous year.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
bone swaging
osseous wall pedicle was placed to treat the infrabony defect by autogrnous bone

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Al-Azhar University

Outcome

Type Measure Description Time frame Safety issue
Primary Radiographic evaluation removing the defect as seen in radiograph defect filling with bone swaging with edta and bone substitute 3 months
Secondary Clinical pocket depth By periodontal prob to measure the clinical parameter 3month
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