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临床试验/RBR-4m7cpb5
RBR-4m7cpb5招募中4 期

Assessment of the quality of anesthesia in patients submitted to ambulatory surgical procedures under sedation with propofol associated with fentanyl or dexmedetomidine: a clinical trial

Empresa Brasileira de Serviços Hospitalares - EBSERH0 个研究点开始时间: 2023年3月6日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方

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
18Y 至 65Y(—)

入选标准

  • Adult patients; aged between 18 and 65 years; undergoing elective outpatient surgical procedures with sedation performed by an anesthesiologist; procedures should be localized and restricted to the skin and subcutaneous tissue; with an expected duration of between 15 minutes and 1 hour; with ASA classification I to IV; who agreed to participate in the study

排除标准

  • Illiterate patients; with some degree of cognitive or mental dysfunction; neurological disease; with a history of allergy to the study drugs; abuse of alcohol and/or illicit drugs or with alterations in renal and/or hepatic function; patients with chronic pain; use of antipsychotic drugs; alpha or beta blockers and/or opioids or who have severe cardiac pathology such as unstable angina; acute myocardial infarction in the last 6 months; heart rate < 50 bpm and systolic blood pressure of 90mmHg; block third-degree atrioventricular or pacemaker; in case of clinical need to use any other medication outside the study protocol or conversion from sedation to general anesthesia

研究者

发起方
Empresa Brasileira de Serviços Hospitalares - EBSERH

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