Sleep Deprivation Clinical Trials
2 recruiting trials for Sleep Deprivation. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Sleep Deprivation clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Pennington Biomedical Research Center (1), University of Utah (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is Time restricted eating (TRE) (behavioral, 1 trial), followed by Central Clock Misalignment, Peripheral Misalignment.
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Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
Cardiovascular Risk and Circadian Misalignment in Short Sleepers - Role of Extended Eating Period
Short sleep duration confers high cardiovascular and metabolic risk, but lifestyle factors and molecular mechanisms that contribute to increased blood pressure and poor glucose...
Nighttime Synchrony of Your Nutrition and Circadian Health
Sleep is an important factor for overall health. This study will see how different light exposure patterns and food intake impact a person's metabolism (how the body breaks down...
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Frequently Asked Questions
There are currently 2 clinical trials for Sleep Deprivation, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Sleep Deprivation, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Sleep Deprivation, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.