Clinical and Radiographic Assessment of the Outcomes of Dental Implant Inserted After Xenograft Socket Preservation in Posterior Maxilla

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

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-01

Study Completion Date

2024-12-01

Brief Summary

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Clinical and Radiographic Assessment of the Outcomes of Dental Implant Inserted after Xenograft Socket Preservation in Posterior Maxilla: A Randomized Controlled Study

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Detailed Description

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Dental implants have become a common choice among the treatment options for missing teeth rehabilitation and has remarkably high survival and success rates Since the introduction of implants into clinical practice more than several decades ago. The success rate of dental implants, over the last ten years, has been about 90- 95%.

Invasive and non-invasive clinical tests are available like histomorphometric analysis, radiographic analysis, push- and pull-out tests, percussion tests, Periotest and resonance frequency analysis (RFA) are employed to assess the steadiness of dental implants to assess objectively implant stability at different stages of its service life to verify successful implantation.

Conditions

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Implant Therapy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This study was conducted on adults above the age of 21 years old with badly decayed posterior maxillary teeth (16 cases) requiring extraction, then subjected to implant placement. These patients were divided equally and http://www.randomizer.org randomly into two groups using Group (A) (8 cases): was treated by immediate socket preservation with S1-XB xenograft augmentation after extraction. Group (B) (8 cases): was not exposed to any type of socket preservation after the extraction procedure.

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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socket preserved

(8 cases): was treated by immediate socket preservation with S1-XB xenograft augmentation after extraction.

Group Type ACTIVE_COMPARATOR

socket preserved

Intervention Type DEVICE

(8 cases): was treated by immediate socket preservation with S1-XB xenograft augmentation after extraction.

non preserved sockets

(8 cases): was not exposed to any type of socket preservation after the extraction procedure.

Group Type PLACEBO_COMPARATOR

non preserved socket

Intervention Type DEVICE

(8 cases): was not exposed to any type of socket preservation after the extraction procedure.

Interventions

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socket preserved

(8 cases): was treated by immediate socket preservation with S1-XB xenograft augmentation after extraction.

Intervention Type DEVICE

non preserved socket

(8 cases): was not exposed to any type of socket preservation after the extraction procedure.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Male patients aged between 21 and 40 years.
* General good health.
* Absence of any relevant systemic disease.
* Presence of a hopeless maxillary posterior tooth that requires extraction.
* Extraction site suitable for replacement by a dental implant.
* Cases have adequate bone width and length.
* Volunteer subjects must sign an informed consent.

Exclusion Criteria

* Poor oral hygiene with no possibility of improvement.
* Smokers (more than 10 cigarettes per day).
* Chronic treatment with any medication known to affect oral status and bone turnover.
* Drug or alcohol abuse.

Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes