Skip to main content
Clinical Trials/NCT04882761
NCT04882761
Completed
Phase 4

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)

Ain Shams University1 site in 1 country16 target enrollmentApril 12, 2017
ConditionsDental Implant

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Dental Implant
Sponsor
Ain Shams University
Enrollment
16
Locations
1
Primary Endpoint
Soft tissue stability
Status
Completed
Last Updated
4 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 12, 2017
End Date
February 24, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Doaa Adel Salah Khattab

Dr

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • 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.
  • Systemic free patients according to modified Cornell medical index (Brodmank and Erdmann 1949).
  • Patients with good compliance.

Exclusion Criteria

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

Outcomes

Primary Outcomes

Soft tissue stability

Time Frame: 6 months postoperatively

Pink esthetic score

Secondary Outcomes

  • Bone stability(6 months postoperatively)

Study Sites (1)

Loading locations...

Similar Trials