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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04824235
Other study ID # alveolar preservation
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 1, 2020
Est. completion date June 1, 2024

Study information

Verified date March 2024
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the present study is to compare the amniotic chorion membrane (ACM) alone versus the amniotic chorion membrane combined with xenograft for their efficacy in alveolar ridge preservation procedures regarding volumetric changes assessed by cone beam computed tomography (CBCT).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date June 1, 2024
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: - Patients require extraction of a non-restorable (premolar or anterior tooth) located in the maxillary arch and needs implant restoration. - Type two sockets will be selected as revealed by Cone beam computed tomography(CBCT) - Absence of any systemic disease or drugs that contraindicate oral surgery using Modified Cornell Medical Index - Male and female within age range of 20-45 years. Exclusion Criteria: - Smokers. - Patients with poor oral hygiene or non-compliant patients who are not willing to perform oral hygiene measures. - Pregnant and breast-feeding females. - Patients with acute peri-apical infection or sinus tract. - Vulnerable group of patients as handicapped patients, orphans,prisoners,etc

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Amniotic Chorion Membrane and Bio-Oss xenograft
Bioxclude Amniotic Chorion Membrane with xenograft (Bio-Oss) for ridge preservation
Amniotic Chorion Membrane only
Bioxclude Amniotic Chorion Membrane only

Locations

Country Name City State
Egypt Ain Shams Faculty of Dentistry Cairo

Sponsors (1)

Lead Sponsor Collaborator
Hams Hamed Abdelrahman

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Bucco-lingual bone width Bone width will be measured using bone caliper and radiographically at baseline, 1 months and 4 months
Primary Change in Corono-apical bone height Bone height using a pre-fabricated stent. at baseline, 1 months and 4 months
Primary total bone volume change It will be evaluated by the use of 3D scans of patient dental models at baseline, and 4 months
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