The Socket Shield Technique, a Prospective Cohort Study of 20 Patients

NCT ID: NCT05902715

Last Updated: 2025-09-05

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

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-06-18

Study Completion Date

2023-01-10

Brief Summary

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

23 implants with socket shield were followed for 18 months. buccal bone thickness and survival rates registered.

Detailed Description

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

Aims: This study aims to collect data on implant survival, bone volume maintenance, and complications associated with the socket shield technique.

Materials \& methods: The study involved the placement of 23 implants using the socket shield technique in 20 patients. AstraTech EV implants were used, and no bone substitutes or connective tissue grafts were applied. Patients were monitored for 18 months, recording implant survival, volumetric bone analysis on CBCT scans, interproximal bone levels, bone sounding, pink esthetic scores, and complications. Prosthetic procedures were also described, including temporary and final restorations.

Conditions

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

Peri-implant Health

Study Design

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

Allocation Method

NA

Intervention Model

SINGLE_GROUP

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.

oral implant placement with socket shield technique

cohort of 20 patients in need of tooth replacement with oral implant

Group Type EXPERIMENTAL

oral implant placement with socket shield technique

Intervention Type DEVICE

tooth is split in socket shield configuration, implant is immediately placed

Interventions

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

oral implant placement with socket shield technique

tooth is split in socket shield configuration, implant is immediately placed

Intervention Type DEVICE

Eligibility Criteria

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

Inclusion Criteria

* • Hopeless teeth suitable for immediate implant placement

* Only single-rooted teeth in the maxilla
* Intact buccal and palatal bone plate
* Intact buccal root portion
* Any periodontal phenotype (thin, thick)

Exclusion Criteria

* • Horizontal root fracture below bone level

* Smoking
* Systemic pathology influencing bone healing
* Active periodontal disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Dentsply Sirona Implants and Consumables

INDUSTRY

Sponsor Role collaborator

Universitaire Ziekenhuizen KU Leuven

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ana CASTRO SARDA

Clinical professor, head of periodontology department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Rutger Dhondt

Role: PRINCIPAL_INVESTIGATOR

Universitaire Ziekenhuizen KU Leuven

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

UZ Leuven

Leuven, , Belgium

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Belgium

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

S59423

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Connective Tissue Graft Versus Collagen Matrix
NCT04210596 ACTIVE_NOT_RECRUITING NA
Immediate Versus Late Placement
NCT04741607 RECRUITING NA