Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05878392
Other study ID # A0103023OS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date January 1, 2023

Study information

Verified date May 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

36 patients, were included in this study. They were chosen from the Outpatient Clinic in the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University for replacement of non-restorable maxillary anterior and premolar teeth (esthetic zone) by immediate implant.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date January 1, 2023
Est. primary completion date June 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Patient medically free from systemic diseases. - Age above 18 years. - A single maxillary anterior or premolar tooth that cannot be restored. - No acute infection is present. - Patients with sufficient quality and quantity of bone. - Free from history of bruxism. Exclusion Criteria: - A medical condition that would prevent implant surgery. - Existence of non-treated generalized progressive periodontitis. - Patients who are smokers.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
bone filling materials
the buccal jumping gap was packed using PRF in group 1 the buccal jumping gap was packed using xenograft in group 2 the buccal jumping gap was packed using Alloplastic ß-tricalcium phosphate in group 3

Locations

Country Name City State
Egypt Heba Elsheikh Mansoura, Egypt

Sponsors (1)

Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary marginal bone loss Cone Beam CT (CBCT) was used measure marginal bone loss 1 year
Secondary Implant Stability: Resonance frequency analysis (RFA) was used to measure implant stability with an Osstell Mentor device. 1 year
Secondary Peri-implant Pocket depth A graduated probe was used to measure the distance between the base of the pocket and the gingival margin 1 year
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06040788 - Effect of Tooth Angulation, Alveolar and Basal Bone Anatomical Characteristics on Soft and Hard Tissue Alterations Around Immediate Implants With Customized Healing Abutment N/A
Not yet recruiting NCT05946954 - Immediate Implant Placement Using Immediate Dentoalveolar Restoration Versus Ice Cream Cone Technique With Labial Plate Dehiscence N/A
Not yet recruiting NCT05891990 - Immediate Implant Placement With Sticky Tooth Versus Autogenous Tooth Graft In Cases With Labial Plate Dehiscence N/A
Completed NCT05020405 - The Effect of Simvastatin With Guided Bone Regeneration in Ridge Splitting and Simultaneously Implantation N/A
Recruiting NCT04489654 - Immediate Implant Using Socket Shield Technique With Xenogenic Bone Graft N/A
Active, not recruiting NCT06241196 - Vestibular Socket Therapy Using Acellular Dermal Matrix Versus Connective Tissue Graft Phase 2
Not yet recruiting NCT05431998 - Evaluation of Autogenous Demineralized Tooth Graft Versus Autogenous Bone Graft During Immediate Implant Placement in the Esthetic Zone. N/A
Completed NCT04731545 - Buccal Bone Resorption in Immediate SLActive Implant Placement Thin vs. Thick Buccal Bone N/A