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Clinical Trials/NCT01602133
NCT01602133
Unknown
N/A

A Clinical Assessment of an Ultrasound-guided Inserted Peripheral Intravenous Catheter

Prodimed SAS1 site in 1 country29 target enrollmentJune 2012
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ConditionsVenous Puncture

Overview

Phase
N/A
Intervention
Not specified
Conditions
Venous Puncture
Sponsor
Prodimed SAS
Enrollment
29
Locations
1
Primary Endpoint
length of use of the catheter measured in number of days
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Evaluate the safety and efficacy of an an ultrasound-guided inserted peripheral intravenous catheter during a period of seven days.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
June 2014
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Prodimed SAS
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Hospitalized patients with need of an intravenous therapy on peripheral line
  • •Unsuccessful attempts at establishing a peripheral intravenous line by nurse
  • •Age over 18 YO
  • •Written informed consent obtained

Exclusion Criteria

  • •pregnant woman
  • •local contra-indication for venous puncture
  • •unconscious patient
  • •need of intravenous therapy requiring central line

Outcomes

Primary Outcomes

length of use of the catheter measured in number of days

Time Frame: seven days

Secondary Outcomes

  • adverse event during the period of use of the catheter(seven days)

Study Sites (1)

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