Anatomy and Ultrasound Evaluation for Central Venous Access

October 26, 2018 updated by: Peking Union Medical College Hospital

Optimisation of Subclavian Venous Catheterization

The anatomy and ultrasound image of subclavian vein was investigated on cadavers, volunteers and patients, respectively. Structures，approach，position and complications were discussed to improve the success rate and safety of central venous catheterization.

Study Overview

Status

Unknown

Conditions

Study Type

Observational

Enrollment (Anticipated)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • China
    • Beijing
      • Beijing, Beijing, China, 100730
        • Recruiting
        • Peking Union Medical College Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

adult Asian without past medical history of the infraclavicular region

Description

Inclusion Criteria:

  • 18-65 years old
  • gender unlimited
  • 18.5 < body mass index (BMI) < 30
  • written consent signed.

Exclusion Criteria:

  • abnormality of the infraclavicular region, including infection, deformity,
  • history of bone, joint, muscle or neurovascular disease
  • history of injury, radiation or invasive procedure
  • subjects refused.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Neutral
abduction
pad
combination

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
area
Time Frame: 12 months
SV area in square centimeter
12 months
length
Time Frame: 12 months
SV length in centimeter
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
width
Time Frame: 12 months
SV width in centimeter
12 months
skin distance
Time Frame: 12 months
depth from skin in centimeter
12 months
comfort
Time Frame: 12 months
comfort level rated by Likert scale ranged point 1 to 5, indicating increased comfort level
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Peking Union Medical College Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2018

Primary Completion (Anticipated)

December 30, 2018

Study Completion (Anticipated)

December 30, 2018

Study Registration Dates

First Submitted

March 22, 2018

First Submitted That Met QC Criteria

March 22, 2018

First Posted (Actual)

March 29, 2018

Study Record Updates

Last Update Posted (Actual)

October 29, 2018

Last Update Submitted That Met QC Criteria

October 26, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • OSCAR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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