Socket Shield With Immediate Implant Stability

Phase 4

Completed

• Conditions: Dental Implant

• Registration Number: NCT04882761
• Lead Sponsor: Ain Shams University

Brief Summary

To evaluate socket shield technique either placing implant in direct contact to tooth fragment versus gap created between the tooth and implant.

Detailed Description

Patients with a non-restorable tooth located in anterior maxillary arch was included in this study, patients were divided into two groups, eight implants per group, both groups had socket shield, group 1 will have implant in direct contact with shield, second group had a gap between dental implant and shield. soft tissue stability, bone width and implant stability was assessed preoperatively, immediate and 6 months postoperative.

Study Timeline

• Study Start: 2017-04-12
• Primary Completion: 2021-01-20
• Study Completion: 2021-02-24
• Study First Submitted: 2021-02-27
• Status Verified: 2021-05
• Study First Submitted QC: 2021-05-06
• Last Update Submitted: 2021-05-06
• Study First Posted: 2021-05-12
• Last Update Posted: 2021-05-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 16

Inclusion Criteria

1. Patients with a non-restorable tooth located in anterior maxillary arch (upper right second premolar to upper left second premolar). Tooth to be extracted is endodontically treated and free from periapical infection.
2. Systemic free patients according to modified Cornell medical index (Brodmank and Erdmann 1949).
3. Patients with good compliance.

Exclusion Criteria

1. Teeth with current acute periapical infection or sinus tracts.
2. Heavy smokers and patients with bruxism habits.
3. Patients with poor oral hygiene or not willing to perform oral hygiene measures.
4. Vulnerable groups (as pregnant females and decisionally impaired individuals).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Soft tissue stability	6 months postoperatively	Pink esthetic score

Secondary Outcome Measures

Name	Time	Method
Bone stability	6 months postoperatively	By Ostell

Trial Locations

Locations (1)

Doaa Khattab; 🇪🇬 Cairo, Abbassia, Egypt