Socket Preservation Using Biodentin Versus Xeno Graft for Single Rooted Teeth

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

RECRUITING

Clinical Phase

PHASE4

Total Enrollment

11 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-12-01

Study Completion Date

2025-12-01

Brief Summary

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socket preservation using biodentin versus xeno graft for single rooted mandibular teeth

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Detailed Description

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after extraction of single rooted mandibular teeth the socket will be filled with xeno graft or biodentine and the socket will be closed using gel foam and sutures then CBCT will be taken to measure bone width after 6 months of healing CBCT will be taken again to measure the difference in bone width and a core biopsy will be taken followed by implant placement

Conditions

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Socket Perservation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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biodentine group

Group Type EXPERIMENTAL

Biodentine

Intervention Type DRUG

biodentine used in socket preservation

xeno graft group

Group Type ACTIVE_COMPARATOR

Biodentine

Intervention Type DRUG

biodentine used in socket preservation

Interventions

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Biodentine

biodentine used in socket preservation

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients of both sex with badly decayed tooth indicated for extraction
* The ages of the patients ranged from 25 to 50 years.
* Patients with healthy systemic condition (Medically free)
* Adequate inter-arch space for placement of the implant prosthetic part.
* Good oral hygiene
* Cooperative patients who are willing to commit for 6 months follow up

Exclusion Criteria

* Subjected to irradiation in the head and neck area less than 1 year before implantation.
* Poor oral hygiene and motivation.
* Smokers
* Patient with medical condition that contraindicates surgical procedures
* Pregnant or nursing.
* Substance abuse.
* Patients with habits that may jeopardize the implant longevity and affect the results of the study such as alcoholism or parafunctional habits severe bruxism or clenching.
* Active infection or severe inflammation in the area intended for implant placement.
* Patients on medication that may interfere with healing (corticosteroids, bisphosphonate, Chemo/radio therapy).

Minimum Eligible Age

25 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No