Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
100

Summary

Conditions
Analgesia
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Younger than 28 years
Gender
Both males and females

Description

Objectives: Principal: validation of the instrument "EVENDOL" in the new-born at term. Secondary: EVENDOL is equivalent to EDIN to diagnose the pain of the newborn at term. While being faster and easier to dimension. EVENDOL preferred by caregivers Methodology and conduct of the study: DESIGN: Study...

Objectives: Principal: validation of the instrument "EVENDOL" in the new-born at term. Secondary: EVENDOL is equivalent to EDIN to diagnose the pain of the newborn at term. While being faster and easier to dimension. EVENDOL preferred by caregivers Methodology and conduct of the study: DESIGN: Study of practical evaluation of observational, prospective, multicenter. Places of study: maternity of Saint Joseph Hospital, and Kremlin Bicetre. A feasibility study is underway, it was started in neonatology Antoine Béclère. Time study: 12 to 18 months Required subjects: 100 patients (1/3 painless children, 2/3 of painful children).

Tracking Information

NCT #
NCT02819076
Collaborators
Not Provided
Investigators
Principal Investigator: Walter Elisabeth, MD Groupe Hospitalier Paris Saint Joseph