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临床试验/NCT04405219
NCT04405219已完成不适用

Preoperative Smoking Cessation, Preoperative Anxiety, Postoperative Anxiety and Pain Relationship

Yuzuncu Yil University4 个研究点 分布在 2 个国家目标入组 120 人开始时间: 2018年2月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120
试验地点
4
主要终点
Anxiety

研究概览

简要总结

Smoking, anxiety and pain are clearly related conditions. We aimed to reveal the relationship between smoking cessation before surgery and preoperative anxiety, postoperative anxiety and pain in chronic smokers.

METHODS ASA I-II group patients without chronic disease and history of drug use were included in the study. Those who did not want to participate in the study, patients with ASA III and above were excluded from the study. The patients were randomized into 2 groups: smokers (Group S, n = 60) and non-smokers (Group NS, n = 60). Group S was asked to quit smoking 2 weeks before the operation. Preoperative period and postoperative 0, 2, 4. And 6. hour Spielberger State-Trait Anxiety Inventory (STAI) values, postop 0., 2., 4., 6. hour Visual Analogue Scale (VAS) values were recorded.

详细描述

it has been revealed in the current study that smoking, pain and anxiety are interrelated with each other. In the preoperative period, high anxiety scores are related to surgery and anesthesia stress. High anxiety scores in the smoker group both in the preoperative period and in the postoperative period are associated with smoking cessation. While the pain scores were similar in the postoperative period, high anxiety scores strengthened the idea of smoking withdrawal and this study gained value. We believe that future studies with a large number of patients, with different parameters and multiple centers will strengthen the results.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Other
盲法
None

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ASA I,II patients
  • planned Rhinoplasti cases
  • accepted participating study

排除标准

  • Patients with chronic systemic disorders,
  • ASA III and above situation
  • emergency and bleeding cases,
  • patients with any cardiac and neurological disorders,
  • refused to participate in the study

结局指标

主要结局

Anxiety

时间窗: 2 hours

assesed with STAI form

次要结局

  • pain scores(2 hours)

研究者

发起方
Yuzuncu Yil University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Arzu Esen Tekeli

Assistant Professor Doctor

Yuzuncu Yil University

研究点 (4)

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