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Assessment of Ultrasound-guided Inserted Peripheral Intravenous Catheter

Not Applicable
Conditions
Venous Puncture
Interventions
Procedure: peripheral venous puncture
Registration Number
NCT01602133
Lead Sponsor
Prodimed SAS
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
29
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
one intervention armperipheral venous puncture-
Primary Outcome Measures
NameTimeMethod
length of use of the catheter measured in number of daysseven days
Secondary Outcome Measures
NameTimeMethod
adverse event during the period of use of the catheterseven days

extravasation and/or catheter removal before the end of the treatment and/or local complications (bleeding, neurologic trouble, venous thrombosis..)

Trial Locations

Locations (1)

Centre Hospitalier Sud Francilien

🇫🇷

Corbeil-essonnes, France

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