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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02809664
Other study ID # 6287
Secondary ID
Status Recruiting
Phase N/A
First received January 4, 2016
Last updated May 15, 2017
Start date October 14, 2015
Est. completion date November 14, 2017

Study information

Verified date May 2017
Source University Hospital, Strasbourg, France
Contact Pierre Kuhn, MD
Phone 33 3 88 12 77 86
Email Pierre.kuhn@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our goal is to demonstrate the feasibility of laying uncomplicated ultrasound-guided central subclavian catheter by supraclavicular route in the newborn.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date November 14, 2017
Est. primary completion date October 14, 2017
Accepts healthy volunteers No
Gender All
Age group 43 Weeks to 44 Weeks
Eligibility Inclusion Criteria:

- Patient hospitalized in the neonatal intensive care or neonatal intensive care at the University Hospital of Hautepierre

- All infants less than 44 weeks corrected age who require a surgical approach

- In the first line if neonate over 34 weeks corrected age requiring dual carriageway catheter

- After Failure or inability laying KTEC for children between 30 and 34 weeks of age corrected and heavy over 1000

Exclusion Criteria:

- Nouveau-né de poids < 1000g

- Nouveau-né de moins de 30 semaines d'âge corrigé

- Choix d'une autre voie d'abord plus judicieux (KTVO, KTC broviac)

- Sortie avant retrait du KTC

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de réanimation néonatale - HOPITAL DE HAUTEPIERRE Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary success rate without complications laying catheter ultrasound guided subclavian by supraclavicular route in newborn 1h after intervention
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