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NCT04882761 Clinical Trial

Socket Shield With Immediate Implant Stability

Dental Implant Clinical Trial

Official title:
Evaluation of Soft Tissue Stability and Labial Plate of Bone of Immediate Implant in Direct Contact Versus Gap With Socket Shield (A Randomized Clinical Study)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04882761
Other study ID # 13875
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 12, 2017
Est. completion date February 24, 2021

Study information
Verified date May 2021
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility
Status Completed
Enrollment 16
Est. completion date February 24, 2021
Est. primary completion date January 20, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 45 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Device:
• Dental implant
Comparative

Locations
Country Name City State
Egypt Doaa Khattab Cairo Abbassia

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Soft tissue stability Pink esthetic score 6 months postoperatively
Secondary Bone stability By Ostell 6 months postoperatively
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