Evaluating the Efficacy and Safety of PROSOMNIA Sleep Therapy™ in Patients With Sleep Deprivation and Chronic Insomnia
Launched by NYREE PENN · Oct 10, 2024
Trial Information
Current as of July 22, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is investigating a new therapy called PROSOMNIA Sleep Therapy (PSTx) for people who struggle with chronic insomnia and sleep deprivation. Chronic insomnia makes it hard to fall asleep or stay asleep, affecting daily life and mood. The trial aims to see if this therapy can improve the quality of REM sleep, which is a vital part of a good night’s rest, by using a medication called Diprivan (Propofol) to induce sleep in a controlled setting. Participants will experience a single therapy session lasting 60 to 120 minutes, during which their brain activity will be monitored to ensure they are getting the right amount of sleep.
To be eligible for the trial, participants should be adults aged 18 to 65 who have chronic insomnia or sleep deprivation and have not found relief with traditional sleep treatments. Those with certain health conditions, like severe obesity or significant heart problems, cannot participate for safety reasons. After the therapy, participants will have follow-up assessments to see how well the treatment worked. This study could offer new hope for people who have struggled to find effective solutions for their sleep issues.
Gender
ALL
Eligibility criteria
- • By adhering to the following criteria, the study aims to select a population that can safely undergo the PROSOMNIA Sleep therapy and for whom the therapy is most likely to be beneficial, ensuring the reliability and validity of the study outcomes.
- INCLUSION CRITERIA:
- • 1. Age Range: 18-65 years of age Reason: This age range includes adults who are most likely to benefit from the PROSOMNIA Sleep therapy and who can provide informed consent. It also excludes children and older adults who may have different physiological responses or additional health risks.
- 2. Diagnosed or Undiagnosed Chronic Insomnia:
- • Reason: Included subjects have a consistent pattern of sleep disturbances that PROSOMNIA Sleep Therapy aims to treat.
- 3. Diagnosed or Undiagnosed Sleep Deprivation:
- • Reason: Includes individuals who are not getting enough sleep quantity, which is a key condition that the PROSOMNIA Sleep Therapy aims to address.
- 4. Diagnosed or Undiagnosed REM Sleep Inconsistencies:
- • Reason: Includes individuals who are not getting enough sleep quality and those with specific REM sleep phase issues that the PROSOMNIA Sleep Therapy is designed to improve.
- 5. Failure to Respond to Conventional Sleep Treatments:
- • Reason: Focuses on subjects who have not found relief from existing sleep therapies, ensuring that the study population represents those in need of alternative solutions.
- 6. Ability to Provide Informed Consent:
- • Reason: Ensures that participants understand the study and agree to participate voluntarily.
- EXCLUSION CRITERIA:
- 1. Severe Obesity (BMI \> 40):
- • Reason: Severe obesity can increase the risk of complications with anesthesia and may affect sleep patterns in ways that could confound study results.
- 2. Cardiovascular Conditions:
- • Reason: Patients with significant heart conditions are at higher risk for complications during anesthesia.
- 3. Neurological Disorders:
- • Reason: These diagnosed conditions and medications such as epilepsy could interfere with sleep patterns and responses to sleep therapy.
- 4. Other Health Conditions Contraindicating Anesthesia:
- • Reason: Includes any condition that would make the use of anesthesia unsafe.
- 5. Greater than ASA II Status:
- • Reason: The American Society of Anesthesiologists (ASA) physical status classification system classifies patients based on their pre-anesthesia medical conditions. Excluding those above ASA II ensures that only patients with mild systemic disease are included, to minimize risks.
- 6. Current Use of Prohibited Medications:
- • Reason: Medications that could interfere with the combined use of anesthesia including, but not limited to sedatives and hypnotics; such as benzodiazepines, Z-drugs and barbiturates.
- 7. Pregnancy or Breastfeeding:
- • Reason: Ensures the safety of the fetus or infant, as the effects of the PROSOMNIA Sleep therapy on pregnancy or lactation are unknown.
About Nyree Penn
Nyree Penn is a dedicated clinical trial sponsor committed to advancing medical research and innovation. With a focus on developing novel therapies and enhancing patient outcomes, Nyree Penn collaborates with leading healthcare professionals and institutions to design and implement high-quality clinical trials. The organization prioritizes ethical standards and regulatory compliance, ensuring that all research activities are conducted with the utmost integrity and respect for patient safety. Through its commitment to scientific excellence and patient-centered approaches, Nyree Penn aims to contribute significantly to the future of healthcare.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Aventura, Florida, United States
Hollywood, Florida, United States
Patients applied
Trial Officials
Nyree Penn, MHSc., CAA, Master of Health Science
Principal Investigator
Memorial Healthcare System
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported