Augmentation of Facial Wall in Defective Fresh Extraction Site for Immediate Implant Placement

NCT ID: NCT06867848

Last Updated: 2025-09-04

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

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-15

Study Completion Date

2025-04-01

Brief Summary

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

The study is performed to clinically and radiographically assess the efficacy of using enriched bone graft combined with slowly resorbable membrane on bone quality in immediate implant placement in extraction socket in cases with localized facial bone defect.

Detailed Description

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

The study is include twelve participants , and the patients are in rolled in two groups, group one receive implant, sticky bone and laminar bone membrane . group two receive implant, sticky bone and pericardium membrane using vestibular incision and 6 months post operative radiographically assessment is performed to measure labial bone quantity formed .

Conditions

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

the Augmentation of Labial Defective Wall in Fresh Extraction Socket

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

the study is interventional study containing two groups, each group receiving deferent type of treatment for their result comparison.
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.

laminar bone membrane

hopeless tooth extraction then immediate implant placed , then by using vestibular incision placing laminar bone membrane under the mucogingival tunnel and fill the gap between the laminar bone membrane and the implant with sticky bone

Group Type EXPERIMENTAL

laminar bone membrane for labial bone augmentation

Intervention Type PROCEDURE

adding laminar bone membrane in one group and pericardium membrane in another group with sticky bone by using vestibular incision in both groups to augment the labial bone over dental implant

pericardium membrane

hopeless tooth extraction then immediate implant placed , then by using vestibular incision placing pericardium membrane under the mucogingival tunnel and fill the gap between the pericardium membrane and the implant with sticky bone

Group Type EXPERIMENTAL

laminar bone membrane for labial bone augmentation

Intervention Type PROCEDURE

adding laminar bone membrane in one group and pericardium membrane in another group with sticky bone by using vestibular incision in both groups to augment the labial bone over dental implant

Interventions

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

laminar bone membrane for labial bone augmentation

adding laminar bone membrane in one group and pericardium membrane in another group with sticky bone by using vestibular incision in both groups to augment the labial bone over dental implant

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

pericardium membrane for labial bone augmentation

Eligibility Criteria

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

Inclusion Criteria

* patient with a single hopeless tooth in maxillary anterior region.
* sufficient bone apically and palatally
* presence of natural contralateral tooth for the tooth being replaced
* systemic healthy patients

Exclusion Criteria

* extraction socket type III
* acute infection in hopeless tooth
* a heavy smoker patient
* pregnant
* had received chemotherapy or radiotherapy in previous year
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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

Nuhayra Ashour Muhammed

OTHER_GOV

Sponsor Role lead

Responsible Party

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

Nuhayra Ashour Muhammed

candidate of master degree in faculty of dental medicine for girls

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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

Faculty of dental medicine for girls

Cairo, , Egypt

Site Status

Countries

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

Egypt

Other Identifiers

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

OR SUR-102-1-E

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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