跳至主要内容
临床试验/CTRI/2026/01/101403
CTRI/2026/01/101403尚未招募不适用

COMPARISON OF SUCCESS OF LONG AXIS VERSUS SHORT AXIS APPROACH FOR ULTRASOUND GUIDED RIGHT INTERNAL JUGULAR VEIN CANNULATION IN ADULT PATIENTS IN INTENSIVE CARE UNIT

JSS ACADEMY OF HIGHER EDUCATION AND RESEARCH1 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2026年1月26日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
106
试验地点
1
主要终点
RIGHT INTERNAL JUGULAR VEIN CANNULATION IN

研究概览

简要总结

•THE INVESTIGATOR WILL APPROACH PATIENTS ADMITTED IN JSS HOSPITAL, IN INTENSIVE CARE UNITS REQUIRING A CENTRAL VENOUS CATHETER.

•AFTER OBTAINING INFORMED CONSENT, THE PARTICIPANT WILL UNDERGO ULTRASOUND GUIDED RIGHT INTERNAL JUGULAR VEIN CANNULATION USING LOGIQ P6 PRO ULTRASOUND MACHINE BY GE HEALTHCARE.

•THE SAMPLE SIZE WILL BE TAKEN AS A TOTAL OF 120 PARTICIPANTS, WITH 60 PARTICIPANTS IN EACH OF THE TWO GROUPS, (MINIMUM OF 53 IN EACH GROUP); CONSIDERING ALPHA ERROR AS 5% AND POWER AS 90%

•SUCCESS OF RIGHT INTERNAL JUGULAR VEIN CANNULATION WILL BE CONSIDERED AS INSERTION OF THE CATHETER AND ASPIRATION OF VENOUS BLOOD IN ALL THE PORTS OF THE CATHETER.

•DURING THE PROCEDURE, THE INVESTIGATOR WILL OBSERVE THE PROCEDURE AND NOTE THE FOLLOWING:

ØFIRST PASS SUCCESS- SUCCESS RATE OF CANNULATION IN SINGLE NEEDLE ATTEMPT.

ØNUMBER OF REDIRECTIONS & PRICKS TAKEN

ØGUIDE WIRE INSERTION TIME (TIME TAKEN FROM NEEDLE INSERTION TO THE ULTRASOUND CONFIRMATION OF PRESENCE OF GUIDEWIRE IN THE VEIN).

ØCATHETER INSERTION TIME (TIME TAKEN FROM ULTRASOUND CONFIRMATION OF PRESENCE OF GUIDEWIRE IN THE VEIN TO THE SUCCESSFUL ASPIRATION OF VENOUS BLOOD FROM ALL THE PORTS OF THE CATHETER).

ØCOMPLICATIONS (IF ANY)- POSTERIOR WALL PUNCTURE, ARTERIAL PUNCTURE, PNEUMOTHORAX, HEMOTHORAX, HEMATOMA FORMATION, ARRHYTHMIAS.

•VITALS & ELECTROCARDIOGRAPHY MONITORING BEFORE, DURING & AFTER THE PROCEDURE.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • PATIENTS AGED MORE THAN 18 YEARS
  • PATIENTS OF EITHER SEX
  • PATIENTS ADMITTED IN INTENSIVE CARE UNIT REQUIRING A CENTRAL VENOUS CATHETER.

排除标准

  • PATIENTS WITH COAGULOPATHY (INR MORE THAN 1.5)
  • PATIENTS WITH INFECTION AT THE SITE OF CANNULATION
  • PATIENTS WITH LESIONS IN THE NECK REGION
  • PATIENTS WHO HAVE UNDERGONE REPEATED INTERNAL JUGULAR VEIN CANNULATION
  • PATIENTS WITH BODY MASS INDEX (BMI) MORE THAN 30
  • PATIENTS NOT WILLING TO PARTICIPATE OR NON-COOPERATIVE PATIENTS.

结局指标

主要结局

RIGHT INTERNAL JUGULAR VEIN CANNULATION IN

时间窗: 18 MONTHS

ADULT PATIENTS IN INTENSIVE CARE UNIT.

时间窗: 18 MONTHS

WE EXPECT THE SHORT AXIS APPROACH

时间窗: 18 MONTHS

TO HAVE A BETTER SUCCESS RATE AS COMPARED TO

时间窗: 18 MONTHS

THE LONG AXIS APPROACH FOR ULTRASOUND GUIDED

时间窗: 18 MONTHS

次要结局

  • COMPARISON OF FIRST PASS SUCCESS RATE AND RATE OF COMPLICATIONS AMONG THE TWO APPROACHES FOR CANNULATION OF RIGHT INTERNAL JUGULAR VEIN IN SINGLE NEEDLE ATTEMPT.(18 MONTHS)

研究者

发起方
JSS ACADEMY OF HIGHER EDUCATION AND RESEARCH
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr UDIT BATHLA

JSS MEDICAL COLLEGE AND HOSPITAL, MYSORE, KARNATAKA

研究点 (1)

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