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.
Investigators
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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