Assessment of Pain Associated With Insertion Torque and Correlation of Primary Implant Stability Measurement Methods
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Dental Implantation
- Sponsor
- Ege University
- Enrollment
- 15
- Primary Endpoint
- Pain levels assessed with the visual analogue scale (VAS)
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
The objective of this observational study is to evaluate the primary stability of dental implants and the relationship between insertion torque and patients' pain levels assessed with the visual analogue scale (VAS)
Detailed Description
Primary implant stability plays a key role in providing osseointegration. Higher insertion torque indicates higher primary stability. However, the effect of increased insertion torque on patient pain levels has not been clearly demonstrated. Several methods for measuring primary stability have been defined so far. Insertion torque, periotest measurements, and resonance frequency analysis are mostly preferred due to their ease of use and non-invasiveness. The aim of the present study is to evaluate the relationship between insertion torque and patients' pain levels assessed with the visual analogue scale (VAS) and to assess the relationship between insertion torque, periotest measurements, and resonance frequency analysis.
Investigators
Mehmet Gumus Kanmaz
DDS
Ege University
Eligibility Criteria
Inclusion Criteria
- •No contraindications for implant surgery;
- •Bilateral single-tooth loss in the posterior mandible;
- •Sufficient bone amount for implant diameter and height at the implant site;
- •At least 3 months after tooth extraction at the implant site;
- •Exclusion Criteria
- •History of chronic infection or pain at the implant site;
- •History of radiotherapy to the head and neck region for any reason;
- •Local or systemic causes of persistent anti-inflammatory or analgesic medication;
- •Patients with suspicion of pregnancy.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Pain levels assessed with the visual analogue scale (VAS)
Time Frame: 7 days
Patients will be asked to record the number of painkillers taken each day and evaluate their pain levels using a 0-10 VAS form before and after the operation. A score of 0 indicated no pain while 10 indicated the worst pain possible. A VAS score of 1-3 indicated mild pain, 4-6 indicated moderate pain, and 7-10 indicated very severe pain.
Secondary Outcomes
- Insertion torque values(1 day)
- Periotest measurements(1 day)
- Resonance frequency analysis values(1 day)