Child and Adolescent Registry for Participants With Narcolepsy
ConditionNarcolepsy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 17
SponsorJazz Pharmaceuticals
About this trial
CATNAP is a patient registry designed to improve the understanding of the natural history of narcolepsy in pediatric patients. Descriptive statistics on disease characteristics will be performed.
The study has 16 active clinical sites and a virtual site that widens participation to anywhere in the United States. For more information about the study or to access the Online Patient Enrollment System, visit the CATNAP website: https://catnap.healthie.net/welcome or email [email protected]. The Online Patient Enrollment System, CATNAP website, can also be found in the references section.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Any child or adolescent with a physician-confirmed diagnosis of narcolepsy
Age less than 18 years
Willing to participate in the Registry and complete the informed consent form
Able to participate in English based registry
Disqualifiers
Age 18 years or more
Fail to complete the informed consent form
Trial population
Any child or adolescent with a physician-confirmed diagnosis of narcolepsy
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Improve Understanding of Natural History of Pediatric Narcolepsy
Time frame
Up to 4 years2
Characterize the Presentation, Identification, and Diagnosis of Narcolepsy in Pediatric Participants
Time frame
Up to 4 years3
Understand Treatment Practices and Outcomes Captured by Treatment Regimen and Rational for Changes
Time frame
Up to 4 yearsSecondary outcomes
1
Improvements in Quality of Life (QoL) as Measured by Epworth Sleepiness Scale for Children and Adolescents (ESS-CHAD) Questionnaire
Time frame
Up to 4 years2
QoL - Pediatric Quality of Life Inventory (PedsQL)
Time frame
Up to 4 years3
Change in frequency of child ehavioral problems utilizing the Child Behavior Checklist (CBCL)
Time frame
Up to 4 years4
Patient Reported Outcomes Measurement Information System (PROMIS) Peer Relationship-Parent Proxy Short Form v2.0
Time frame
Up to 4 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov