跳至主要内容
临床试验/CTIS2022-500377-13-01
CTIS2022-500377-13-01招募中1 期

Randomized clinical trial to evaluate the utility of CYP2D6 genotyping to improve the efficacy and safety of tramadol in the treatment of acute postoperative pain - 1

Fundacion Para La Investigacion Biomedica Del Hospital Universitario La Princesa0 个研究点目标入组 300 人开始时间: 2022年4月18日最近更新:
适应症

试验速览

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • 1. Men or women over 18 years of age., 2. Patients scheduled for outpatient surgical extraction, under local anesthesia, of at least two impacted third molars, at least one of which will require bone removal., 3. Patients who agree to participate in the study and give written consent.

排除标准

  • 1. Patients under treatment with other drugs that can inhibit CYP2D6, or are contraindicated in combination with tramadol or dexketoprofen., 2. Patients on treatment with bisphosphonates., 3. Patients who are receiving analgesic treatment before the operation, 24 hours prior to the operation. This criterion will be evaluated at the intervention visit., 4. Patients suffering from other uncontrolled diseases., 5. Pregnant or breastfeeding women., 6. Patients with contraindications for treatment with tramadol or dexketoprofen.

研究者

相似试验