NCT05107089

Brief Summary

  1. 1.To observe and report the success rate associated with the use of ultrasound for subclavian vein catheterization.
  2. 2.To observe and report the type and complications and any constrains associated with this technique.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Nov 2021

Typical duration for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 25, 2021

Completed
7 days until next milestone

Study Start

First participant enrolled

November 1, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

November 4, 2021

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

November 4, 2021

Status Verified

October 1, 2021

Enrollment Period

3 years

First QC Date

October 25, 2021

Last Update Submit

October 25, 2021

Conditions

Outcome Measures

Primary Outcomes (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

    Use of ultrasound at visualization of cannulation of subclavian vein

    Baseline

Interventions

Use of ultrasound at subclavian vein cannulation for visualization

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Any patient has arrived to the emergency room with sign of hypovolemic shock Or arrested

You may qualify if:

  • All patient admitted to emergency room and indicated for central venous catheterization

You may not qualify if:

  • \. Any contraindication for central vein cannulation as coagulopathy, hemorrhage from target vessel, suspected proximal vascular injury 2- Age below 18 year

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Hayashi M, Oshima K. Purification and properties of oxytocinase (cystine amino-peptidase) from monkey placenta. J Biochem. 1976 Aug;80(2):389-96. doi: 10.1093/oxfordjournals.jbchem.a131288.

    PMID: 12146BACKGROUND

MeSH Terms

Interventions

Ultrasonography

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Central Study Contacts

Alshaima R Mohamed, Resident

CONTACT

Khaled S Mostafa, Professor

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident

Study Record Dates

First Submitted

October 25, 2021

First Posted

November 4, 2021

Study Start

November 1, 2021

Primary Completion

November 1, 2024

Study Completion

March 1, 2025

Last Updated

November 4, 2021

Record last verified: 2021-10