Alveolar Ridge Preservation Using Amniotic Chorion Membrane
Not Applicable
Completed
- Conditions
- Alveolar Ridge Preservation
- Interventions
- Other: Amniotic Chorion Membrane onlyOther: Amniotic Chorion Membrane and Bio-Oss xenograft
- Registration Number
- NCT04824235
- Lead Sponsor
- Hams Hamed Abdelrahman
- Brief 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).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
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
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Amnoitic Chorion Membrane only Amniotic Chorion Membrane only extraction sockets where ridge preservation will be performed using Chorion Membrane Alone Amnoitic Chorion Membrane and xenograft Amniotic Chorion Membrane and Bio-Oss xenograft extraction sockets where ridge preservation will be performed using Chorion Membrane with Xenograft
- Primary Outcome Measures
Name Time Method Change in Bucco-lingual bone width at baseline, 1 months and 4 months Bone width will be measured using bone caliper and radiographically
Change in Corono-apical bone height at baseline, 1 months and 4 months Bone height using a pre-fabricated stent.
total bone volume change at baseline, and 4 months It will be evaluated by the use of 3D scans of patient dental models
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Ain Shams Faculty of Dentistry
🇪🇬Cairo, Egypt