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Active, Not Recruiting

NCT Number: NCT03142893

Hormonal Mechanisms of Sleep Restriction - Axis Study

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Conditions

Age range

22 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Los Angeles Biomedical Research Institute

Torrance, California, 90509, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men aged 22-45 years
  • Willingness to provide written informed consent
  • Stable weight over preceding 6 weeks
  • Body Mass index (BMI) 20-28 kg/m2

Exclusion criteria

  • Unable or unwilling to provide IRB (Internal Review Board)-approved informed consent
  • Clinical disorders and/or illnesses
  • Current medical or drug treatment, as assessed by questionnaire
  • History of brain injury or of learning disability - Vision or hearing impairment unless corrected back to normal
  • Anemia (Hct <38%)
  • History of psychiatric illness
  • Clinically significant abnormalities in blood and urine, and free of traces of drugs
  • Other endocrine abnormalities including hypothyroidism or adrenal failure; primary gonadal disease as indicated by serum LH (luteinizing hormone) or FSH (follicle stimulating hormone) concentration >10 or >15 IU/L, respectively, hyperprolactinemia indicated by prolactin >25ug/L
  • Type 2 Diabetes (HgbA1C)
  • Current smoker
  • Recent or concurrent drug or alcohol abuse
  • Blood donation in previous eight weeks
  • Travel across time zones within one month of entering the study
  • Sleep or circadian disorder
  • Shift work within three months of entering the study
  • Irregular bedtimes (not between 6 and 10 hours in duration)
  • Unoperated obstructive uropathy, recurrent prostatitis, indeterminate prostatic nodularity, Hx or Suspicion of cancer of the prostate gland or PSA (prostate-specific antigen) >4ng/ml
  • Previous adverse reaction to sleep deprivation or any of the drugs to be administered
  • Concurrent participation in another research study

Treatment and study plan

Ketoconazole Pill

Drug

Ketoconazole pill is taken 4 times per Inpatient Stay

Other names: Nizoral

Ganirelix

Drug

Ganirelix subcutaneous injection is administered twice per Inpatient Stay

Dexamethasone

Drug

Dexamethasone Pills is taken twice per Inpatient Stay

Dexamethasone Injection

Drug

Dexamethasone IV injection is given twice per Inpatient Stay

Cosyntropin Injectable Product

Drug

cosyntropin injection is given twice per Inpatient Stay

Recombinant Human Luteinizing Hormone

Drug

Leutinizing-Releasing Hormone is given 6 IV infusion pulses per Inpatient Visit

Other names: Luveris

Hydrocortisone Injection

Drug

Hydrocortisone IV push is given twice per Inpatient Visit

Other names: solu-cortef

Gonadorelin

Drug

Gonadorelin IV injection is given twice per Inpatient Stay

Other names: Lutrepulse

Corticorelin

Drug

Corticorelin IV injection is given twice per Inpatient Stay

Other names: Acthrel

Placebo oral capsule

Drug

Placebo for ketoconazole are given 4 times per Inpatient Stay

Saline Solution

Drug

Saline Solution (Placebo) for Dexamethasone IV injection or hydrocortisone IV injection given up to four times per Inpatient Stay

Saline Solution for Injection

Drug

Saline Solution (placebo) for ganirelix subcutaneous injection

Primary outcomes

  1. Average Blood Cortisol Concentration

    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.

  2. Average Blood Testosterone Concentration

    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.

Secondary outcomes

  1. Peak Blood Cortisol Concentration

    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.

  2. Peak Blood Testosterone Concentration

    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.

  3. Trough Blood Cortisol Concentration

    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.

  4. Trough Blood Testosterone Concentration

    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.

  5. Reaction time on Psychomotor Vigilance Task

    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.

  6. Karolinska Sleepiness Scale

    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.

  7. Two card gambling task

    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'.

  8. Modified Sternberg working memory test

    Time frame: 5 days

    Computerized neurobehavioral testing to determine how 4 nights of sleep restriction affects reaction time and accuracy.

  9. Caloric Intake

    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.

  10. Hunger Scale

    Time frame: 5 days

    Hunger scale using Flint visual analogue scale to assess how 4 nights of sleep restriction affects participants' appetite.

  11. Food Cravings

    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.

Sponsors and collaborators

Lead sponsor

Peter y. Liu

Other

Registry information

Important dates

Study start
2017
Primary completion
2020
Study completion
2026
First posted
May 8, 2017
Registry last updated
Sep 11, 2025

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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