Los Angeles Biomedical Research Institute
Torrance, California, 90509, United States
NCT Number: NCT03142893
The purpose of this study is to 1) determine how hypothalamic-pituitary-adrenal axis (HPA axis) activation occurs with sleep restriction 2) evaluate how hypothalamic-pituitary-gonadal axis (HPG axis) deactivation occurs with sleep restriction. The investigator will also examine the cognitive function associated with sleep restriction, including food intake and food cravings.
This study is active but is not currently recruiting participants.
22 year–45 year
Male
Interventional
Phase 1
Torrance, California, 90509, United States
Sleep restriction increases evening cortisol and decreases testosterone. These are the main catabolic and anabolic hormones in men, respectively. This catabolic-anabolic imbalance likely leads to metabolic and reproductive ill-health. The hypothalamic-pituitary-end organ (adrenal or testis) mechanisms that must underpin these changes are unknown. This study will administer drugs to clamp the function of each of these nodes to determine the regulatory changes that have occurred with sleep restriction. Even though the study is randomized order in design, the main comparison is before and after sleep restriction under each of these clamp conditions. Participants are admitted to the chronobiology laboratory where they are given 1 night of 10 hours sleep opportunity, followed by 4 nights of 4 hours sleep opportunity. Up to 80 participants (assuming twenty different participant for each of the 4 clamp conditions) can be enrolled. However, participants will be allowed an opportunity to be randomized to all 4 conditions so that as few as 20 participants may be required. Urn randomization will be used to ensure that 20 different participants are involved in each of the 4 conditions.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ketoconazole pill is taken 4 times per Inpatient Stay
Other names: Nizoral
Ganirelix subcutaneous injection is administered twice per Inpatient Stay
Dexamethasone Pills is taken twice per Inpatient Stay
Dexamethasone IV injection is given twice per Inpatient Stay
cosyntropin injection is given twice per Inpatient Stay
Leutinizing-Releasing Hormone is given 6 IV infusion pulses per Inpatient Visit
Other names: Luveris
Hydrocortisone IV push is given twice per Inpatient Visit
Other names: solu-cortef
Gonadorelin IV injection is given twice per Inpatient Stay
Other names: Lutrepulse
Corticorelin IV injection is given twice per Inpatient Stay
Other names: Acthrel
Placebo for ketoconazole are given 4 times per Inpatient Stay
Saline Solution (Placebo) for Dexamethasone IV injection or hydrocortisone IV injection given up to four times per Inpatient Stay
Saline Solution (placebo) for ganirelix subcutaneous injection
Time frame: 5 days
Cortisol is measured in blood every 10 minutes for a 5 hour period, at the beginning and at the end of 4 nights of sleep restriction. The average cortisol is the parameter of interest.
Time frame: 5 days
Testosterone is measured in blood every 10 minutes for a 5 hour period, at the beginning and at the end of 4 nights of sleep restriction. The average cortisol is the parameter of interest.
Time frame: 5 days
This is the single maximal blood cortisol concentration that is measured during the entire 5 hour period, at the beginning and at the end of 4 nights of sleep restriction.
Time frame: 5 days
This is the single maximal blood testosterone concentration that is measured during the entire 5 hour period, at the beginning and at the end of 4 nights of sleep restriction.
Time frame: 5 days
This is the single minimal blood cortisol concentration that is measured during the entire 5 hour period, at the beginning and at the end of 4 nights of sleep restriction.
Time frame: 5 days
This is the single minimal blood testosterone concentration that is measured during the entire 5 hour period, at the beginning and at the end of 4 nights of sleep restriction.
Time frame: 5 days
This is measured by lapses in attention. As the person becomes more sleepy, there are more lapses (reaction time >500 ms), at the beginning and at the end of 4 nights of sleep restriction.
Time frame: 5 days
Measures how sleepy participants are using a scale of 1 (extremely alert) through 9. This scale will be used to assess changes in sleepiness throughout the day and through 4 nights of sleep restriction.
Time frame: 5 days
Computerized neurobehavioral testing to determine how 4 nights of sleep restriction affects participants' decision making. The end point is discriminability index, d'.
Time frame: 5 days
Computerized neurobehavioral testing to determine how 4 nights of sleep restriction affects reaction time and accuracy.
Time frame: 5 days
The food given to participants is weighed. The amount that is not consumed is also weighed. The difference in weight is the amount of calories consumed.
Time frame: 5 days
Hunger scale using Flint visual analogue scale to assess how 4 nights of sleep restriction affects participants' appetite.
Time frame: 5 days
Food cravings is measured using Food Cravings Index scale to assess which food groups participants have cravings for and how their cravings change during 4 nights of sleep restriction.
Peter y. Liu
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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