Immediate and Delayed Implant Placement Using Socket Shield Technique and Autogenous Dentin Graft

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-17

Study Completion Date

2023-12-19

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

One of the techniques that have been proposed to reduce the amount of bone resorption in anterior maxilla is the "socket shield (SS) ". This technique includes preservation of the facial segment of a root to be extracted and immediate implant placement. A technique of socket shield with delayed implantation using autogenous dentin graft for socket preservation, as an alternative to autogenous bone grafts, has shown predictable clinical and histological outcomes.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Socket Preservation Using Socket Shield Technique Comparison of Socket Preservation Using Socket Shield Technique With Autogenous Dentin Graft Versus Alloplast Graft Material

NCT05047887

Extraction Tooth Socket

COMPLETED NA

Injectable Platelet-rich Fibrin and Advanced Platelet-rich Fibrin With Xenograft on the Socket Preservation of Mandibular Extracted Molars

NCT06936358

Tooth Extraction Socket Preservation

COMPLETED NA

Effect of Hyaluronic Acid, With Demineralized Tooth Graft, in Socket Preservation, vs Demineralized Tooth Graft Alone.

NCT05613075

Alveolar Bone Resorption Socket Preservation Bone Resorption +1 more

COMPLETED NA

Elamrousy Novel Approach of Socket Shield Technique

NCT06263842

Implant Complication

COMPLETED NA

Elamrousy Modified Approach for Socket Shield Technique

NCT06043037

Implant Site Reaction Tooth Extraction Status Nos Dental Implant Failed

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dental Implant Tooth Loss Socket Shield

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group A

Group Type EXPERIMENTAL

Immediate implant

Intervention Type OTHER

Immediate Implant with Socket Shield Group

Group B

Group Type ACTIVE_COMPARATOR

Delayed implant

Intervention Type OTHER

Delayed Implant with Socket preserved with socket Shield and dentin graft Group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Immediate implant

Immediate Implant with Socket Shield Group

Intervention Type OTHER

Delayed implant

Delayed Implant with Socket preserved with socket Shield and dentin graft Group

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients with badly destructed or non-restorable maxillary anterior teeth when the Labial cortical plate is still intact, and the thickness was found to be \<2mm in CBCT.
* Patients with health status according to American Society of Anesthesiology (ASA) I and II.
* Patients who agree to participate in the study.

Exclusion Criteria

* Patients presenting with any systemic pathology or health condition that would inhibit the osseointegration process of the implants.
* Perforated labial cortical plate seen in CBCT.
* Patients undergoing radiation therapy or history of radiation within the last two years.
* Drug or alcohol abuse

Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No