Clinical Trials Logo

Narcolepsy clinical trials

View clinical trials related to Narcolepsy.

Filter by:

NCT ID: NCT05627388 Not yet recruiting - Narcolepsy Clinical Trials

Feasibility Study of At-Home EEG Monitoring for Hypersomnia

Start date: February 2023
Phase: N/A
Study type: Interventional

The central hypothesis is that home EEG monitoring (Dream 3 wearable) can be feasibly utilized for data capture of continuous sleep and wake measurements for the diagnostic evaluation and treatment monitoring of hypersomnia.

NCT ID: NCT05615584 Not yet recruiting - Narcolepsy Clinical Trials

Spectrometry (MRM) Versus I 125 Radioimmunoassay (RIA) for Quantification of Orexin-A of Patients With Hypersomnolence

MRM-OREX
Start date: January 30, 2023
Phase: N/A
Study type: Interventional

In humans, selective loss of orexin neurons is responsible for type 1 narcolepsy (NT1), or narcolepsy with cataplexy, or orexin deficiency syndrome. The International Classification of Sleep Disorders 3rd edition (ICSD-3) distinguishes between hypersomnolence of central origin: NT1, narcolepsy type 2 (NT2), or narcolepsy without cataplexy, and idiopathic hypersomnia (HI). These rare conditions are all characterised by hypersomnolence (excessive daytime sleepiness, or excessive need for sleep), which is the primary and often most disabling symptom. A level of ORX-A in cerebrospinal fluid (CSF) (<110 pg/mL) is a very sensitive and specific biomarker of NT1, currently sufficient for the diagnosis of this condition. In contrast, ORX neurons are thought to be intact in IH and NT2, and the pathophysiological mechanisms underlying these diseases remain unknown. Thus, their diagnosis is based solely on clinical and electrophysiological criteria. The objective of this project is to determine the validity of a mass spectrometric technique for the determination of ORX-A in the cerebral spinal fluid of patients suffering from hypersomnolence in comparison with the radioimmunoassay which is the reference technique.

NCT ID: NCT05536011 Recruiting - Pregnancy Related Clinical Trials

WAKIX® (Pitolisant) Pregnancy Registry

Start date: August 24, 2021
Phase:
Study type: Observational [Patient Registry]

The WAKIX (pitolisant) Pregnancy Registry is a US-based, prospective, observational cohort study designed to evaluate the association between pitolisant exposure during pregnancy and subsequent maternal, fetal, and infant outcomes.

NCT ID: NCT05530447 No longer available - Narcolepsy Clinical Trials

Expanded Access to SUVN-G3031 (Samelisant) for the Treatment of Subjects With Narcolepsy

Start date: n/a
Phase:
Study type: Expanded Access

The study is planned to provide expanded access treatment to subjects with narcolepsy who have completed the 2-week treatment phase and follow-up in study CTP2S13031H3 (NCT04072380), and in instances when the investigator as well as the subject believe that the benefits outweigh the risks to continue the treatment with SUVN-G3031.

NCT ID: NCT05460052 Completed - Narcolepsy Type 1 Clinical Trials

Evaluation of the Effectiveness of a Physical Activity Program on the Severity of Narcolepsy

NARCOSPORT
Start date: August 26, 2022
Phase:
Study type: Observational

Narcolepsy Type 1 (NT1) is a rare chronic neurological disorder resulting from the selective loss of hypocretin neurons. Patients with NT1 suffer from excessive daytime sleepiness, disrupted nighttime sleep, and cataplexy (emotionally triggered episodes of muscle atonia). The disease is associated with numerous comorbidities such as obesity, metabolic disorders, anxiety-depressive disorders, and attentional disorders, all of which have a strong impact on quality of life.

NCT ID: NCT05375890 Completed - Narcolepsy Type 1 Clinical Trials

Clinical and Neurophysiological Characteristics of Narcolepsy

Start date: November 1, 2019
Phase:
Study type: Observational [Patient Registry]

The study is the first attempt in post-Soviet Russian history to collect and analyze the existing available data of narcolepsy cohort in order to get prove characteristics of narcolepsy in Russia according to known data. Investigators created the system of national narcolepsy centers in Russia - Russian narcolepsy network, with a purpose of collecting clinical and neurophysiological data with subsequent analyze and formation of Russian narcolepsy profile.

NCT ID: NCT05373979 Recruiting - Clinical trials for Obstructive Sleep Apnea

Development and Validation of Pediatric Narcolepsy Patient Reported Outcomes Scale

PN-PROS
Start date: April 2, 2019
Phase:
Study type: Observational

The purpose of this study is to test a pediatric narcolepsy patient reported outcomes tool to assess pediatric narcolepsy symptoms and their effect on daily functioning and quality of life. The goal is to develop a clinical survey that can improve the care of pediatric narcolepsy.

NCT ID: NCT05371483 Enrolling by invitation - Narcolepsy Clinical Trials

Cardiovascular and Cognitive Implications of Central Disorders of Hypersomnolence and Their Treatments

Start date: May 18, 2022
Phase:
Study type: Observational

This is an observational study evaluating patients diagnosed with narcolepsy or idiopathic hypersomnia that have been prescribed a new/different hypersomnia treatment. The study is being done to better understand how hypersomnia treatment(s) impact blood pressure and cognitive function.

NCT ID: NCT05321355 Recruiting - Insomnia Clinical Trials

Mainz Register of Patients With Sleep Disorders

MAINZ-SLEEPREG
Start date: February 1, 2022
Phase:
Study type: Observational [Patient Registry]

Prospective longitudinal observational registry study of all patients with sleep disorders treated in the Mainz Comprehensive Epilepsy and Sleep Medicine Center with the focus on the course of the disease and quality of life.

NCT ID: NCT05314556 Completed - Narcolepsy Type 1 Clinical Trials

Group Psychotherapy in Narcolepsy Type 1

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

The aim of this pilot study is to test the benefit of behavior therapy-oriented, method-integrated psychotherapy in an outpatient group setting in patients with narcolepsy type 1. Therefore we collect and evaluate initial data on its effectiveness on the disease in terms of specific symptomatology, emotion regulation, health-related quality of life, and disease processing/acceptance.