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临床试验/NCT02766829
NCT02766829已完成不适用

Comparison of Successful Spinal Needle Placement Between Crossed Leg Sitting Position and Traditional Sitting Position in Patients Underwent Urology Surgery

Indonesia University1 个研究点 分布在 1 个国家目标入组 211 人开始时间: 2015年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
211
试验地点
1
主要终点
One shot successful spinal needle placement

研究概览

简要总结

The study aimed to compare successful spinal needle placement between crossed leg sitting position and traditional sitting position in patients underwent urology surgery.

详细描述

Approval from Ethical Committee of Faculty of Medicine Universitas Indonesia was acquired prior conducting the study. Subjects were given informed consent before enrolling the study. Subjects were randomly divided into CLSP Group for crossed leg sitting position (n=105) and TSP Group for traditional sitting position (n=106). Non-invasive blood pressure (NIBP) monitor, eletrocardiography (ECG), oxygen nasal cannula and pulse-oxymetry was set on the subjects in the operation room. Baseline information was recorded. Spinal anesthesia was done by anesthesiology registrars that have done 50 spinal anesthesia procedures and have been explained about the protocol of spinal anesthesia injection in this study (to avoid bias). Outcome measures were the number of successful spinal needle placement in the first attempt, the difficulty level of landmark palpation for injection, and the number of needle-bone contact. Data was analyzed by SPSS (Statistical Package for Social Scientist) using Chi-Square test, Fisher Exact test, and Kolmogorov-Smirnov test. Significance value used was 5% with 80% power.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • •subjects aged 18-60 years old-
  • •subjects with ASA physical status I-III who were planned to undergo urology surgery with spinal anesthesia
  • •Subjects who have been explained about the study, have agreed to enroll and have signed the informed consent form

排除标准

  • •uncooperative subjects
  • •subjects with relative and absolute contraindications to spinal anesthesia (coagulation disorders, thrombocytopenia, increases intracranial pressure, severe hypovolemia, severe heart valve disorders, local infection at the injection site, allergy toward local anesthetic agents, significant anatomical disorder of the spine, wound/scar on the lumbal area)
  • •subjects with body mass index (BMI) > 32 kg/m2
  • •Drop out criteria:
  • •subjects who requestes to drop out of the study
  • •subjects in need of emergency treatment during spinal anesthesia procedure
  • •subjects with more than nine times redirected spinal needle (failed spinal anesthesia procedure).

研究组 & 干预措施

TSP Group

Active Comparator

Those with traditional sitting position: patient is positioned with her knees flexed 90o, both feet hanging of the bed and propped up by a chair, both arms hugging a pillow, adducted pelvic, maximum pelvic flexion were done to create maximal sagittal lumbal flexion.

干预措施: Traditional sitting position (Procedure)

CLSP Group

Experimental

Those with cross leg sitting position: patients sit with both their knees flexed medially, hip flexed, resulting in pelvic leaning posteriorly and reducing lumbal lordosis.

干预措施: Cross leg sitting position (Procedure)

结局指标

主要结局

One shot successful spinal needle placement

时间窗: 7 months

The number of successful spinal needle placement in the first attempt

Needle-bone contact number

时间窗: 7 months

The number of needle-bone contact recorded.

The difficulty level of landmark palpation for injection

时间窗: 7 months

the difficulty level of landmark palpation for injection were assessed as easy or difficult.

次要结局

  • Spinal needle placement complications(7 months)

研究者

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

Sidharta K. Manggala

Consultant, Anesthesiologist

Indonesia University

研究点 (1)

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