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临床试验/NCT03268278
NCT03268278终止1 期

Efficacy of Buprenorphine on Postoperative Endodontic Analgesia

University Hospitals Cleveland Medical Center1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2017年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
终止
入组人数
10
试验地点
1
主要终点
The Efficacy of Buprenorphine in addition to Local Anesthetic in Providing Prolonged Postoperative Endodontic Analgesia

研究概览

简要总结

To see whether the addition of buprenorphone to local anesthesia will lengthen postoperative analgesia for endodontic pain

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • persons with preoperative pain to percussion of a tooth with pulpal disease requiring endodontic therapy, healthy individuals, ASA Class I and II, no known allergies to the drugs being administered

排除标准

  • pregnancy, allergy to buprenorphine, allergy to local anesthetic

研究组 & 干预措施

buprenorphine and local anesthetic

Active Comparator

buprenorphine added to local anesthetic

干预措施: Buprenorphine (Drug)

buprenorphine and local anesthetic

Active Comparator

buprenorphine added to local anesthetic

干预措施: lidocaine, epinephrine (Local anesthetic) (Drug)

sterile saline and local anesthetic

Placebo Comparator

sterile saline (placebo) added to local anesthetic

干预措施: Sterile saline (Drug)

sterile saline and local anesthetic

Placebo Comparator

sterile saline (placebo) added to local anesthetic

干预措施: lidocaine, epinephrine (Local anesthetic) (Drug)

结局指标

主要结局

The Efficacy of Buprenorphine in addition to Local Anesthetic in Providing Prolonged Postoperative Endodontic Analgesia

时间窗: two years

The number of patients with extended postoperative analgesia when compared to the baseline in pain scores on a visual analog scale during a three-day period will be analyzed. A questionnaire containing a visual analog scale and a log for recording the use of rescue analgesics will be used to gather the data.

次要结局

未报告次要终点

研究者

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

Thomas A. Montagnese

Associate Professor

University Hospitals Cleveland Medical Center

研究点 (1)

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