Status:

COMPLETED

Kisspeptin Administration in the Adult

Lead Sponsor:

Massachusetts General Hospital

Conditions:

Hypogonadotropic Hypogonadism

Kallmann Syndrome

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

The goal of this study is to learn about the role of kisspeptin in the reproductive system. Kisspeptin is a naturally occurring hormone in humans that causes the release of other hormones, including g...

Detailed Description

The reproductive hormone GnRH is essential for normal reproductive function. People with idiopathic hypogonadotropic hypogonadism (IHH), hyperprolactinemia, and polycystic ovarian syndrome (PCOS) do n...

Eligibility Criteria

Inclusion

  • A. Healthy Subjects
  • All healthy subjects will meet the following criteria:
  • normal puberty with respect to onset and pace,
  • no chronic diseases,
  • no difficulty with blood draws,
  • no prescription medications for at least 2 months with the exception of seasonal allergy medications and hormone replacement therapy,
  • no illicit drug use or excessive alcohol consumption (\< 10 drinks/week),
  • no history of a medication reaction requiring emergency medical care,
  • normal physical exam and laboratory studies within protocol reference ranges.
  • Additional criteria based on subject population:
  • Healthy Men:
  • between 21 and 40 years old,
  • normal erectile and ejaculatory function, no history of reproductive disorders,
  • testicular volume \>15 ml.
  • Healthy women:
  • between 21 and 40 years old,
  • not breastfeeding or pregnant,
  • menstrual cycles between 25 and 35 days in duration, at least 11 periods/year, with no more than 5 days variability in cycle duration,
  • no evidence for androgen excess (hirsutism or acne),
  • at screening, negative hCG pregnancy test,
  • negative screening for Factor V Leiden for those who might receive estradiol treatment as a part of this study.
  • Healthy postmenopausal women:
  • between 50 and 60 years old,
  • no menstrual periods within the last year,
  • previous history of menstrual cycles between 25 and 35 days in duration, with no more than 5 days variability in cycle duration,
  • if applicable, able to undergo washout from hormone therapy,
  • no evidence for androgen excess (hirsutism or acne),
  • negative screening for Factor V Leiden for those who might receive estradiol treatment as a part of this study.
  • B. Subjects with Reproductive Disorders
  • All subjects with reproductive disorders will meet the following criteria:
  • 18 years or older,
  • all medical conditions stable and well controlled,
  • no prescription medications known to affect reproductive endocrine function for at least 2 months except for medications used to treat the subject's reproductive condition,
  • no history of a medication reaction requiring emergency medical care,
  • no illicit drug use or excessive alcohol consumption (\<10 drinks/week),
  • for women, not breastfeeding or pregnant,
  • if applicable, able to undergo appropriate washout from hormone therapy,
  • normal physical exam and laboratory studies within protocol reference ranges,
  • for women, at time of screening negative hCG pregnancy test.
  • Additional criteria based on subject population:
  • Men and women with hypogonadotropic hypogonadism,
  • Confirmed diagnosis by low sex steroids in the setting of low or inappropriately normal gonadotropins,
  • If needed, additional labs and imaging tests may be performed.
  • Women with Polycystic Ovarian Syndrome (PCOS)
  • Confirmed diagnosis of PCOS,
  • If needed, additional labs and imaging tests may be performed.
  • Men and women with hyperprolactinemia
  • confirmed diagnosis of elevated levels of prolactin measured via blood test,
  • no pituitary adenoma OR a microprolactinoma (\<10 mm). Patients with a macroprolactinoma confirmed on MRI imaging will be excluded,
  • willing to complete a dopamine agonist washout.

Exclusion

    Key Trial Info

    Start Date :

    June 23 2009

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    October 22 2021

    Estimated Enrollment :

    256 Patients enrolled

    Trial Details

    Trial ID

    NCT00914823

    Start Date

    June 23 2009

    End Date

    October 22 2021

    Last Update

    July 31 2024

    Active Locations (1)

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    Massachusetts General Hospital

    Boston, Massachusetts, United States, 02114