Alveolar Ridge Preservation Clinical Trial
Official title:
Alveolar Ridge Preservation Using Amniotic Chorion Membrane Alone or Combined With Xenograft (A Randomized Controlled Clinical Trial With Histological Evaluation)
Verified date | March 2024 |
Source | Alexandria University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
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 |
Country | Name | City | State |
---|---|---|---|
Egypt | Ain Shams Faculty of Dentistry | Cairo |
Lead Sponsor | Collaborator |
---|---|
Hams Hamed Abdelrahman |
Egypt,
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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