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临床试验/NCT06176287
NCT06176287已完成不适用

Assessment of Pain Associated With Insertion Torque and Correlation of Primary Implant Stability Measurement Methods

Ege University0 个研究点目标入组 15 人开始时间: 2016年4月19日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
15
主要终点
Pain levels assessed with the visual analogue scale (VAS)

研究概览

简要总结

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)

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 未提供

结局指标

主要结局

Pain levels assessed with the visual analogue scale (VAS)

时间窗: 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.

次要结局

  • Insertion torque values(1 day)
  • Periotest measurements(1 day)
  • Resonance frequency analysis values(1 day)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mehmet Gumus Kanmaz

DDS

Ege University

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