MedSleep is a leader in conducting research and clinical trials with the goal of advancing the treatment options in sleep medicine.
Our clinical trials are conducted in compliance with International Conference on Harmonisation (ICH)-Good Clinical Practice (GCP), regulatory guidance and standard operating procedures.
Our highly skilled staff includes clinical research coordinators, a patient recruitment specialist and board registered polysomnographic technologists.
In addition, we have a full-time medical director/principal investigator and more than 20 consulting physicians with specialties in sleep medicine, psychiatry, psychology, neurology, respirology and internal medicine.
MedSleep clinical research has the following advantages:
For more information, contact us at email@example.com.
You may qualify to participate in any of our clinical research studies if you meet the study criteria.
This study will be used to create a database on sleep related data, which will include genetic and phenotype data to gain a better understanding of the genetic architecture of sleep and to help improve the detection, treatment and prevention of sleep disorders.
To qualify for this study, participants must:
Qualified participants will receive:
We are currently seeking volunteers who may be interested in participating in a clinical trial involving an investigational medication (a medication that is being tested).
To qualify, you must:
If you qualify for any of these clinical studies, you may receive the following:
Call or email us so we can discuss further whether you would be eligible for any of the clinical trials.
Please note that if you do not qualify for a research study at this time, you can still enter your information to be included in our database to be contacted for any future research trials for which you may qualify.ac
Research Trial Application
Please complete the form below and click the Submit button if you would like to be put on a list to be contacted when the next trial begins.