Impact on Patient Satisfaction About Realization of Ultrasound Dopplers at the Bed

February 12, 2019 updated by: Groupe Hospitalier Paris Saint Joseph

Organisation and logistic about realisation of vascular doppler ultrasound is something very eclectic . Need to shift patient from their bed , long waiting time and the effect on the hospital cost.

That's why vascular yard aim to practise these doppler ultrasound directly in the patients' room in the bed.

And like that evaluate the patient's satisfaction of this kind of coverage.

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Study Type

Observational

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

patients hospitalized in vascular yard of GHPSJ

Description

Inclusion Criteria:

  • hospitalized in vascular yard
  • indication of ultrasound doppler
  • accept to participate

Exclusion Criteria:

  • refuse to participate
  • without ultrasound doppler indication.

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
Intervention / Treatment
echo doppler at the bed
Procedure: echo doppler at the bed
we practise the echo doppler at the patient 's bed
echo doppler in the vascular exploration platform
Procedure: echo doppler in the vascular exploration platform
as usual , practising echo doppler in the medical platform

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
score of a satisfaction questionnaire
Time Frame: 24 hours
in the current practice every patient fill up a questionnaire named SAPHORA to evaluate their satisfaction
24 hours

Collaborators and Investigators

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

Sponsor

Groupe Hospitalier Paris Saint Joseph

Investigators

  • Study Director: PRIOLLET Pascal, MD, GHPSJ

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)

February 2, 2017

Primary Completion (Actual)

June 30, 2017

Study Completion (Actual)

December 31, 2018

Study Registration Dates

First Submitted

October 16, 2017

First Submitted That Met QC Criteria

October 23, 2017

First Posted (Actual)

October 25, 2017

Study Record Updates

Last Update Posted (Actual)

February 15, 2019

Last Update Submitted That Met QC Criteria

February 12, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • SAPHODOPPLER

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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