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临床试验/NCT06786013
NCT06786013已完成不适用

Effects of Interscalene Block Anesthesia on Visual Clarity and Hemodynamic Parameters in Arthroscopic Rotator Cuff Repair: A Prospective, Randomized Study

Konya Necmettin Erbakan Üniversitesi1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年1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
80
试验地点
1
主要终点
Visual clarity during arthroscopic rotator cuff repair

研究概览

简要总结

Arthroscopic rotator cuff repair (RCR) has become the predominant technique for managing patients with full-thickness rotator cuff tears. Optimizing visual clarity is crucial for performing shoulder arthroscopy safely, precisely, and successfully. However, intraoperative bleeding remains the most significant factor impairing visual clarity.

The interscalene brachial plexus block (ISB) technique is widely employed in shoulder joint and upper extremity surgeries. However, ISB may lead to hypertension due to the spread of local anesthetic to adjacent structures, such as the carotid sinus baroreceptors. Hypertension-induced microbleeding can obstruct the surgical field of view.

Our hypothesis suggests that arthroscopic visual clarity may be compromised in awake patients receiving ISB for anesthesia.

This study aims to compare the effects of interscalene brachial plexus block and general anesthesia on hemodynamic parameters and visual clarity in patients undergoing arthroscopic rotator cuff repair surgery.

详细描述

Our study will be conducted prospectively, and no additional medication or interventional procedure will be administered to the patients. A total of 80 patients, 40 from the general anesthesia group and 40 from the interscalene block anesthesia group, who meet the inclusion criteria, will be included in the study. In both groups, systolic arterial blood pressure (SAB), diastolic arterial blood pressure (DAB), mean arterial blood pressure (MAP), and heart rate (HR) values will be recorded every 5 minutes throughout the operation after the surgical procedure begins. At the end of the operation, visual clarity will be assessed by the same surgeon (M.O) using a Numeric Rating Scale (0 = very poor, 10 = excellent). To detect a 2-point (20%) difference in the NRS score for visual clarity, a total of 37 patients are required with 80% power and a significance level of 0.05. This calculation assumes that such an effect is clinically significant and that the standard deviation is 2.21. Assuming a 10% dropout rate, we calculated that a total of 80 patients would be needed for two groups, with 40 patients per group.

Descriptive statistics, including mean, standard deviation, median, minimum, maximum, frequency, and percentage, will be used to summarize the data. The Kolmogorov-Smirnov test will be employed to assess the distribution of variables. For the comparison of quantitative data, the Independent Samples t-test and Mann-Whitney U test will be utilized. For the comparison of qualitative data, the Chi-Square test will be used. A p-value less than 0.05 will be considered statistically significant.

The cut-off values of quantitative parameters will be determined using ROC analysis.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients able to provide informed consent.
  • •Patients able to reliably report their symptoms to the research team.
  • •ASA physical status classification of 1-
  • •Scheduled to undergo arthroscopic rotator cuff repair surgery in the lateral decubitus position.

排除标准

  • •Contraindications to anesthesia.
  • •Patients under 18 years old.
  • •Cognitive impairment or communication barriers.
  • •Weight less than 50 kg or more than 100 kg.
  • •Psychiatric disorders.
  • •Chronic opioid therapy for pain.
  • •Severe liver, heart, or kidney failure.
  • •Hypertension (possibly severe, depending on the study context).
  • •Use of opioids for any reason.
  • •Revision shoulder surgery.
  • •Diaphragmatic paralysis on the opposite side of the planned intervention.
  • •Concurrent anticoagulation therapy or coagulopathy.
  • •Skin deformities or infections in the block area.
  • •Progressive neurological deficits affecting peripheral nerves.
  • •Allergy to amide-structured local anesthetics.
  • •ASA physical classification score ≥
  • •Suspected or confirmed pregnancy.
  • •Breastfeeding mothers.
  • •Patients who do not consent to participate in the study.

结局指标

主要结局

Visual clarity during arthroscopic rotator cuff repair

时间窗: 1 day

Visual clarity of the arthroscopic view will be assessed by the same surgeon (MO) using a Numeric Rating Scale (0 = very poor, 10 = excellent).

次要结局

  • Hemodynamic parameters(1 day)
  • Visual analog scale (VAS) pain scores(at 6,12, 18, 24 hours postoperatively)

研究者

发起方
Konya Necmettin Erbakan Üniversitesi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alper Kilicaslan

Alper Kılıçaslan, MD, Prpf, Specialist in Anesthesiology and Reanimation.

Konya Necmettin Erbakan Üniversitesi

研究点 (1)

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