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Clinical Trials/IRCT20160315027056N2
IRCT20160315027056N2
Completed
Phase 3

An evaluation to compare peri-implant crevicular fluid cytokine level using intact manufacturer or reused healing abutments: A controlled clinical trial

Vice Chancellor for Research and Technology, Kerman University of Medical Sciences0 sites50 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Vice Chancellor for Research and Technology, Kerman University of Medical Sciences
Enrollment
50
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Vice Chancellor for Research and Technology, Kerman University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Age of the patient should be over 18
  • Implant treatment should be performed in patients with partial or complete edentulous
  • Bone level implant placement in one stage and obtaining suitable primary stability should be possible.
  • Good patient compliance, reference for follow\-up visits and observation of post operation instructions should also be possible.

Exclusion Criteria

  • Patients who have periodontal disease
  • Conditions that affect the immune system such as diabetes and pregnancy
  • The habit of smoking and alcohol or tobacco consumption
  • History of Antibiotics, anti\-inflammatory, and immunosuppressive drugs intake three months before the study.

Outcomes

Primary Outcomes

Not specified

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