Ultrasound Guided Subclavian Vein Cannulation at Emergency Room

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05107089
Collaborator
(none)
30
40

Study Details

Study Description

Brief Summary

  1. To observe and report the success rate associated with the use of ultrasound for subclavian vein catheterization.

  2. To observe and report the type and complications and any constrains associated with this technique.

Condition or Disease Intervention/Treatment Phase
  • Device: Ultrasound

Detailed Description

Central venous catheterisation is a commonly performed procedure in anaesthesia, critical care, acute and emergency medicine. 1 , the subclavian vein (SCV) has been an important vessel for central venous cannulation.2 The SCV cannulation offers several advantages when compared to the common alternative sites for central venous access. These advantages may include fewer cases of thrombosis, infectious complications, better patient comfort, and increased ability to remain patent in hypovolemic states.3-4 Traditionally, subclavian venous catheterisation has been performed using the landmark technique and because of the complications associated with this technique, it is not commonly performed.1 the complications such as catheter malposition, arterial puncture, hematoma, pneumothorax, hemothorax, and nerve injury.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Ultrasound Guided Subclavian Vein Cannulation at Emergency Room , Success Rate and Incidence of Complications
Anticipated Study Start Date :
Nov 1, 2021
Anticipated Primary Completion Date :
Nov 1, 2024
Anticipated Study Completion Date :
Mar 1, 2025

Outcome Measures

Primary Outcome Measures

  1. success rate of the ultrasound guided subclavian vein cannulation success rate of the ultrasound guided subclavian vein cannulation Success rate of ultrasound guided of subclavian vein cannulation [Baseline]

    Use of ultrasound at visualization of cannulation of subclavian vein

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • All patient admitted to emergency room and indicated for central venous catheterization
Exclusion Criteria:
    1. Any contraindication for central vein cannulation as coagulopathy, hemorrhage from target vessel, suspected proximal vascular injury 2- Age below 18 year

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
ARMohamed, Resident, Assiut University
ClinicalTrials.gov Identifier:
NCT05107089
Other Study ID Numbers:
  • Subclavian vein cannulation
First Posted:
Nov 4, 2021
Last Update Posted:
Nov 4, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 4, 2021