Observational Study of LUMRYZ in Narcolepsy
Completed
Conditions studied: Narcolepsy
In brief
This is an observational study of LUMRYZ prescribed in clinical practice. Patients are asked if they would be willing to complete questionnaires over a 4-month period after starting LUMRYZ. The questionnaires ask about narcolepsy symptoms, experience with LUMRYZ, and quality of life.
Key facts
- Study ID
- NCT06792708
- Run by
- Avadel
- People needed
- 71
- Starts
- 2024-07-18
- Expected to finish
- 2025-10-28
- Last updated by the study team
- 2026-02-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults with narcolepsy
- Oxybate naive or prior treatment with twice-nightly oxybate
- Access to smart phone, tablet or laptop with reliable internet connection
- Able to read/understand English
- Written informed consent and ability to comply with schedule
You may not qualify if…
- Already using LUMRYZ
- Clinical or mental health condition excluded by LUMRYZ label
- Any other condition/situation that would adversely impact participation
Where it is running
- Jeremy D McConnell, MD PA — Bradenton, Florida, United States
- Comprehensive Sleep Center — East Lansing, Michigan, United States
- Patient First MD — Middletown, New Jersey, United States
- Ghaly Sleep Management Services — East Syracuse, New York, United States
- University Hospitals Cleveland Medical Center — Cleveland, Ohio, United States
- Ohio Sleep Medicine Institute — Dublin, Ohio, United States
- Abington Neurological Associates — Abington, Pennsylvania, United States
- Pulmonology Associates, Inc. — Wynnewood, Pennsylvania, United States
- Respiratory Specialists — Wyomissing, Pennsylvania, United States
- Bogan Sleep Consultants — Columbia, South Carolina, United States
- Tricoastal Narcolepsy and Sleep Disorder Center — Sugar Land, Texas, United States
- Northwest Houston Neurology — Tomball, Texas, United States
Full record on ClinicalTrials.gov
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