RecruitingACTRN12606000223538

Comparison of success rate, speed of insertion and acute complication rates of central venous catheter (CVC) insertion between using ultrasound guidance technique and traditional anatomical landmark technique in elective surgery


Sponsor

Department of Anaesthesia, St Vincent's Hospital , Melbourne

Enrollment

190 participants

Start Date

May 8, 2006

Study Type

Interventional

Conditions

Summary

A prospective randomised controlled trial to assess the potential benefits and acute complication rates of ultrasound guided CVC insertion with traditional anatomical landmark insertion technique


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study is comparing two methods for inserting a central venous catheter (CVC) — a thin tube placed into a large vein in the neck or chest, commonly needed during major surgery. The two methods are: (1) using ultrasound to guide the needle, and (2) using traditional anatomical landmarks (relying on feel and knowledge of body structure). Researchers want to find out which method is faster, more successful on the first try, and causes fewer complications. You may be eligible if: - You are 18 years or older - You are scheduled for a planned (elective) CVC insertion in an operating theatre You may NOT be eligible if: - Your CVC insertion was not planned in advance (unplanned emergency insertion) - You have a history of difficult CVC insertion - You have a known neck abnormality Talk to your doctor about whether this trial might be right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Central venous catheter (CVC) insertion by using ultrasound guidance technique in the immediate perioperative period of elective surgery

Central venous catheter (CVC) insertion by using ultrasound guidance technique in the immediate perioperative period of elective surgery


Locations(1)

Australia

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ACTRN12606000223538