Immediate Implant With Different Filling Materials

Immediate Implant Clinical Trial

Official title:

Comparison Between Different Filling Materials in Immediate Implant

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05878392
• Other study ID #: A0103023OS
• Status: Completed
• Phase: N/A
• 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
• 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.

Related Conditions & MeSH terms

• Immediate Implant

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