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FASS (Facial Action Summary Score) Scale to Differentiate the Pain of Postoperative Anxiety in Children Under 7 Years (FASS)

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ClinicalTrials.gov Identifier: NCT02483338
Recruitment Status : Unknown
Verified June 2015 by University Hospital, Montpellier.
Recruitment status was:  Recruiting
First Posted : June 26, 2015
Last Update Posted : July 9, 2015
Sponsor:
Information provided by (Responsible Party):
University Hospital, Montpellier

Brief Summary:
This study aims to evaluate the psychometric validity of FASS (Facial Summary Score Scale) to assess postoperative children pain.

Condition or disease Intervention/treatment Phase
Postoperative Pain Behavioral: Assessment of pain Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 150 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Does the FASS (Facial Action Summary Score) Scale Allow to Differentiate the Pain of Postoperative Anxiety in Children Under 7 Years?
Study Start Date : July 2011
Estimated Primary Completion Date : December 2015
Estimated Study Completion Date : December 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anxiety

Arm Intervention/treatment
Children surgery Behavioral: Assessment of pain
Assessment of pain using FASS but without using this score to manage pain




Primary Outcome Measures :
  1. FASS (Facial Action Summary Score) [ Time Frame: As soon as the child arrive in recovery room or / and the extubation, before and after the administration of analgesics ]


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Ages Eligible for Study:   up to 7 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Children surgery
  • Younger than 7 years old
  • Elective surgery
  • Patient whose parents will have given their non-opposition

Exclusion Criteria:

  • Psychological retardation
  • Chronic pain

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02483338


Contacts
Contact: Sophie SB BRINGUIER, HP 0467337960 ext 0033 s-bringuierbranchereau@chu-montpellier.fr

Locations
France
University hospital Lapeyronie Recruiting
Montpellier, France, 34295
Contact: Sophie SB BRINGUIER, HP    0467337960 ext 0033    s-bringuierbranchereau@chu-montpellier.fr   
Sponsors and Collaborators
University Hospital, Montpellier
Investigators
Principal Investigator: Sophie SB BRINGUIER, HP Department of Anesthesia Resuscitation at the Hospital Lapeyronie in Montpellier

Responsible Party: University Hospital, Montpellier
ClinicalTrials.gov Identifier: NCT02483338     History of Changes
Other Study ID Numbers: 8824
2011-A00533-38 ( Registry Identifier: ID-RCB )
First Posted: June 26, 2015    Key Record Dates
Last Update Posted: July 9, 2015
Last Verified: June 2015

Keywords provided by University Hospital, Montpellier:
Psychometric validity
Pain scale
Postoperative
Children

Additional relevant MeSH terms:
Pain, Postoperative
Pain
Neurologic Manifestations
Nervous System Diseases
Postoperative Complications
Pathologic Processes
Signs and Symptoms