Alveolar Ridge Preservation Using Amniotic Chorion Membrane

NCT ID: NCT04824235

Last Updated: 2025-01-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-01

Study Completion Date

2024-06-01

Brief Summary

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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

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Conditions

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Alveolar Ridge Preservation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Amnoitic Chorion Membrane and xenograft

extraction sockets where ridge preservation will be performed using Chorion Membrane with Xenograft

Group Type EXPERIMENTAL

Amniotic Chorion Membrane and Bio-Oss xenograft

Intervention Type OTHER

Bioxclude Amniotic Chorion Membrane with xenograft (Bio-Oss) for ridge preservation

Amnoitic Chorion Membrane only

extraction sockets where ridge preservation will be performed using Chorion Membrane Alone

Group Type ACTIVE_COMPARATOR

Amniotic Chorion Membrane only

Intervention Type OTHER

Bioxclude Amniotic Chorion Membrane only

Interventions

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Amniotic Chorion Membrane and Bio-Oss xenograft

Bioxclude Amniotic Chorion Membrane with xenograft (Bio-Oss) for ridge preservation

Intervention Type OTHER

Amniotic Chorion Membrane only

Bioxclude Amniotic Chorion Membrane only

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hams Hamed Abdelrahman

OTHER

Sponsor Role lead

Responsible Party

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Hams Hamed Abdelrahman

Assistant lecturer of DPH and Clinical statistician

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Ain Shams Faculty of Dentistry

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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alveolar preservation

Identifier Type: -

Identifier Source: org_study_id

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