Study Results
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.
COMPLETED
NA
8 participants
INTERVENTIONAL
2019-10-01
2020-06-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Customized Healing Abutments on Peri-implant Soft Tissue and Bone
NCT06125418
Immediate Functional Versus Non Functional Implant Loading in the Mandible
NCT04521530
Comparative Clinical Study of Conventional vs Customized Healing Abutments in Dental Implantology
NCT07031232
Evaluation of the Abutment Type Following Oral Implants in Terms of the Surrounding Bone Height
NCT05350293
Stability and Crestal Bone Changes Around Implants Placed at Crestal Versus Subcrestal Level in Controlled Type Two Diabetic Patients
NCT05125445
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The aim of this study is to evaluate clinically and radiographically the effect of customized healing abutment on peri-implant osteogenesis following immediate implant placement.
A clinical trial was carried out on 8 patients (20-40 years old) with freshly extracted mandibular molars. Implants were placed immediately after extraction and a customized healing abutment will be fabricated. Patients were followed up clinically and radio graphically for 6 months.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
immediate implant with customized healing abutment
immediate implant with customized healing abutment
* All patients will be operated under local anesthesia.
* Atraumatic extraction of the remaining root or tooth will be achieved.
* A careful curettage of the socket will be performed if any granulation tissue is present.
* Sequential drilling of the osteotomy site with copious irrigation will be done
* The Implant is secured in place using a torque wrench.
* Fabrication of the customized abutment with flowable composite by first placing a rubber dam between the abutment and the implant to prevent leakage of composite into the socket then start adding the composite in a manner to seal the socket.
* Finishing the composite outside the patient's mouth will be done to ensure the borders are smooth with no sharp ends.
* The abutment will be attached to the implant.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
immediate implant with customized healing abutment
* All patients will be operated under local anesthesia.
* Atraumatic extraction of the remaining root or tooth will be achieved.
* A careful curettage of the socket will be performed if any granulation tissue is present.
* Sequential drilling of the osteotomy site with copious irrigation will be done
* The Implant is secured in place using a torque wrench.
* Fabrication of the customized abutment with flowable composite by first placing a rubber dam between the abutment and the implant to prevent leakage of composite into the socket then start adding the composite in a manner to seal the socket.
* Finishing the composite outside the patient's mouth will be done to ensure the borders are smooth with no sharp ends.
* The abutment will be attached to the implant.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Good oral hygiene
* A freshly extracted socket in the mandibular molar area.
* The gap between the implant and the bone will be at least 3-4 mm.
Exclusion Criteria
* Patients on radiotherapy or chemotherapy.
* Alcohol or drug abuse.
* Patient with the systemic disorder (uncontrolled Diabetes mellitus, autoimmune diseases, bone diseases, etc.)
* Smokers.
* Parafunctional habits.
20 Years
40 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hams Hamed Abdelrahman
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hams Hamed Abdelrahman
Assistant lecturer of DPH and Clinical statistician
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of Dentistry
Alexandria, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Immediate implants
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.