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Alveolar Ridge Preservation Using Amniotic Chorion Membrane

Not Applicable
Completed
Conditions
Alveolar Ridge Preservation
Interventions
Other: Amniotic Chorion Membrane only
Other: 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
GroupInterventionDescription
Amnoitic Chorion Membrane onlyAmniotic Chorion Membrane onlyextraction sockets where ridge preservation will be performed using Chorion Membrane Alone
Amnoitic Chorion Membrane and xenograftAmniotic Chorion Membrane and Bio-Oss xenograftextraction sockets where ridge preservation will be performed using Chorion Membrane with Xenograft
Primary Outcome Measures
NameTimeMethod
Change in Bucco-lingual bone widthat baseline, 1 months and 4 months

Bone width will be measured using bone caliper and radiographically

Change in Corono-apical bone heightat baseline, 1 months and 4 months

Bone height using a pre-fabricated stent.

total bone volume changeat baseline, and 4 months

It will be evaluated by the use of 3D scans of patient dental models

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ain Shams Faculty of Dentistry

🇪🇬

Cairo, Egypt

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