PRADER-WILLI SYNDROME
Prader-Willi Syndrome (PWS) is a congenital syndrome that affects many systems of the body. Common early signs of PWS include muscle weakness, feeding difficulties, and behavioral disturbances. Patients may also experience excessive daytime sleepiness (EDS), making it difficult to perform everyday activities and negatively affecting their mood. The purpose of this study is to evaluate the efficacy and safety of the study medication on daytime sleepiness in those with Prader-Willi Syndrome.
STUDY: Evaluate the efficacy and safety of the study medication on daytime sleepiness in those with Prader-Willi Syndrome (PWS).
At Santa Monica Clinical Trials, we are actively recruiting qualified participants for a study evaluating the effectiveness and safety of a study treatment for sleep disturbances in individuals with Prader-Willi Syndrome. If you are interested and available, please contact us today.
​
-
Length of trial: up to 1 year
-
Age range: 2 - 65 years of age
-
Treatment: The effectiveness and safety of an oral investigational drug that affects sleep in individuals with Autism Spectrum Disorder.
​
All of our clinical trials are performed at no cost to you. No medical insurance is necessary and you may be compensated for your participation.
MOTION SICKNESS
Motion sickness is a common condition affecting about 30% of the population. Common symptoms of motion sickness include nausea, vomiting, stomach awareness, pallor, headache, sweating, dizziness, a sensation of warmth and drowsiness. The purpose of the study is to evaluate the effectiveness of an investigational drug on symptoms associated with motion sickness and to assess the safety of the investigational drug.
STUDY: EVALUATE THE EFFECTIVENESSÂ OF AN INVESTIGATIONAL DRUG ON DELAYED SLEEP WAKE-PHASE DISORDER.
At Santa Monica Clinical Trials, we are actively recruiting qualified participants for a study evaluating the effectiveness and safety of a study treatment for delayed sleep wake-phase disorder. If you are interested and available, and you meet the qualifications outlined below, please contact us today.
​
Length of trial: 5-8 weeks, with an option to participate in an additional 11 months extension phase
Age range: 16-65 years of age
Treatment: The effectiveness and safety of an oral investigational drug that affects delayed sleep wake-phase disorder.
​
All of our clinical trials are performed at no cost to you. No medical insurance is necessary and you may be compensated for your participation.
WHAT TO EXPECT
A clinical trial is scientific research designed to test if a medication or medical device is effective and well-tolerated for use by people.
PRE-SCREEN
First, a phone conversation is performed between the study volunteer and a member of the research staff to determine if the volunteer would be a good fit for the study.
SCREENING VISIT
Following pre-screen eligibility, the study volunteer visits the clinic to learn the details of the study that are outlined in the Informed Consent Form and begins participation in the study.
RANDOMIZATION VISIT
After successfully enrolling in the study, the study volunteer is randomized into a study treatment group either consisting of placebo or the investigational product.
STUDY VISITS
Every study has its own established number of clinic visits, phone call visits, and/or at-home visits which are performed throughout the duration of the study. These visits may include lab draws, questionnaires, or exams depending on the study protocol.
POST-TREATMENT FOLLOW UP
After successful completion of the clinical trial, the study volunteer will either visit the clinic or have a phone call visit to record any changes in the participant's health.