NCT03456141已完成不适用
Prospective, Observational Study With a Multimodal Analgesic Protocol to Moderate Acute Pain After Third Molar Surgery
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- The impact of the surgery on the patient's post-surgery pain.
研究概览
简要总结
With a prospective, observational study assess post-surgery pain levels and patient's use of opioids and other analgesic drugs to moderate pain following third molar surgery.
详细描述
SPECIFIC AIMS Using the UNC surgery clinic multi-modal protocol of drugs/dosages to control acute pain after third molar surgery assess each post-surgery day(PSD) the patient reported
- pain levels post-surgery as recorded by Likert-type and Gracely scales
- quality of life(QOL) outcomes for lifestyle and oral function
- number of opioid doses taken by subject-patients
- number of NSAID and acetaminophen doses taken by subject-patients.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 35 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •ASA I,II At least two lower 3rd molars scheduled for removal
排除标准
- •Patient being treated for opioid addiction/abuse including having Rx for suboxone, methadone
结局指标
主要结局
The impact of the surgery on the patient's post-surgery pain.
时间窗: 14 days
Likert scales for average pain and worst pain are assessed with 7-point scales with verbal anchors of "no pain" and "worst pain imagined". Recovery for pain on the Likert scales is defined as the number of PSD until the patient reports a score of 1 or 2 on the 7-point scale.
次要结局
未报告次要终点
研究者
研究点 (1)
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