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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04899947
Other study ID # HealhieCATNAPN.A.
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 10, 2020
Est. completion date October 1, 2024

Study information

Verified date May 2024
Source Jazz Pharmaceuticals
Contact Director Clinical Trial Disclosure & Transparency
Phone 2158709177
Email ClinicalTrialDisclosure@JazzPharma.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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 catnap@pulseinfoframe.com. The Online Patient Enrollment System, CATNAP website, can also be found in the references section.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date October 1, 2024
Est. primary completion date October 1, 2024
Accepts healthy volunteers No
Gender All
Age group N/A to 17 Years
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - Age 18 years or more - Fail to complete the informed consent form

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Johns Hopkins University Baltimore Maryland
United States Boston Children's Hospital Boston Massachusetts
United States St. Luke's Hospital Chesterfield Missouri
United States Lurie Children's Hospital of Chicago Chicago Illinois
United States Cincinnati Children's Hospital Medical Center Cincinnati Ohio
United States University Hospitals Cleveland Medical Centre (UHCMC) Cleveland Ohio
United States Nationwide Children's Hospital Columbus Ohio
United States Geisinger Danville Pennsylvania
United States Ohio Sleep Medicine Institute Dublin Ohio
United States University of Arkansas Fayetteville Arkansas
United States Trinity Health-Michigan Grand Rapids Michigan
United States Texas Children's Hospital (Baylor College of Medicine) Houston Texas
United States Children's Mercy Hospital Kansas City Missouri
United States Arkansas Children's Research Institute Little Rock Arkansas
United States Northwell Health Manhasset New York
United States Children's Hospital of the King's Daughters Norfolk Virginia
United States Children's Hospital of Philadelphia Philadelphia Pennsylvania
United States Phoenix Children's Hospital Phoenix Arizona
United States Stanford University Redwood City California
United States Mayo Clinic Rochester Michigan
United States University of California San Diego San Diego California
United States University of South Florida Tampa Florida
United States University of Arizona Tucson Arizona
United States Children's National Medical Center Washington District of Columbia
United States Children's Research Institute Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Jazz Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improve Understanding of Natural History of Pediatric Narcolepsy Up to 4 years
Primary Characterize the Presentation, Identification, and Diagnosis of Narcolepsy in Pediatric Participants Up to 4 years
Primary Understand Treatment Practices and Outcomes Captured by Treatment Regimen and Rational for Changes Up to 4 years
Secondary Improvements in Quality of Life (QoL) as Measured by Epworth Sleepiness Scale for Children and Adolescents (ESS-CHAD) Questionnaire Up to 4 years
Secondary QoL - Pediatric Quality of Life Inventory (PedsQL) Up to 4 years
Secondary Change in frequency of child ehavioral problems utilizing the Child Behavior Checklist (CBCL) Up to 4 years
Secondary Patient Reported Outcomes Measurement Information System (PROMIS) Peer Relationship-Parent Proxy Short Form v2.0 Up to 4 years
Secondary Caregiver Work Limitations Questionnaire (C-WLQ) Up to 4 years
Secondary Work Productivity and Activity Impairment (WPAI) Up to 4 years
Secondary Change in Caregiver Well-being Measured by the Caregiver Well-Being Scale (Shortened) Up to 4 years
Secondary Change in Level of Social Support using the Social Support Survey Instrument Up to 4 years
Secondary Change in Pittsburgh Sleep Quality index (PSQI) scores Up to 4 years
See also
  Status Clinical Trial Phase
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Withdrawn NCT03626727 - Evaluation of the Efficacy of Sodium Oxybate (Xyrem®) in Treatment of Post-traumatic Narcolepsy and Post-traumatic Hypersomnia Early Phase 1
Completed NCT02821715 - Safety and Efficacy of THN102 on Sleepiness in Narcoleptic Patients Phase 2
Completed NCT01681121 - A Study of the Safety and Effectiveness of ADX-N05 for Excessive Daytime Sleepiness in Subjects With Narcolepsy Phase 2
Completed NCT01789398 - Patient Narcoleptic Treated With BF2.649 (Pitolisant) in add-on to Sodium Oxybate (HARMONY IV) Phase 3
Completed NCT00174174 - Provigil (Modafinil) Study by Taiwan Biotech Co. N/A
Completed NCT05059223 - A Study to Assess the Efficacy and Safety of AXS-12 (Reboxetine) in Patients With Narcolepsy Phase 3
Completed NCT04923594 - Four-week Study of the Safety and Efficacy of NLS-2 (Mazindol Extended Release) in the Treatment of Narcolepsy Phase 2
Recruiting NCT06279247 - Proteomics and Metabolomics of Body Fluid in Patients With Narcolepsy
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Completed NCT03267303 - A Study to Evaluate the Safety and Efficacy of TS-091 in Patients With Narcolepsy Phase 2
Completed NCT03173378 - Evaluation of Academic and Professional Trajectories of Narcoleptic Patients
Completed NCT05055024 - An Open Label Study of NLS-2 (Mazindol Extended Release) in Subjects With Narcolepsy Phase 2
Completed NCT01067235 - Efficacy and Safety Study of BF2.649 and BF2.649 Add on Modafinil on Cataplexy in Patients With Narcolespy Phase 3
Completed NCT00228566 - Study to Assess Patient Reported Outcomes With Armodafinil Treatment for Excessive Sleepiness in Adults With Narcolepsy or Obstructive Sleep Apnea/Hypopnea Syndrome Phase 3
Completed NCT00132873 - Trial of Xyrem® (Sodium Oxybate) for the Treatment of Narcolepsy Phase 3
Completed NCT00107796 - Study of PROVIGIL ® (Modafinil) Treatment in Children and Adolescents With Excessive Sleepiness Associated With Narcolepsy Phase 3
Completed NCT00107848 - PROVIGIL® (Modafinil) Treatment in Children and Adolescents With Excessive Sleepiness Associated With Narcolepsy or Obstructive Sleep Apnea/Hypopnea Syndrome Phase 3
Enrolling by invitation NCT05113745 - A Study to Assess the Long-term Efficacy and Safety of AXS-12 (Reboxetine) in Subjects With Narcolepsy Phase 3
Suspended NCT04419792 - 'A Profile of Physical Performance Variables in an Out-patient Adult Population With Narcolepsy'