Completed

Gonadotropin-Releasing Hormone Pulse Frequency in Sexual Maturation and Menstrual Cycle Study

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Who is being recruted

Bone Diseases+17

+ Bone Diseases, Developmental

+ Bone Diseases, Endocrine

From 7 to 35 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: April 1993
See protocol details

Summary

Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Study start date: April 1, 1993

Actual date on which the first participant was enrolled.

PROTOCOL OUTLINE: This project involves several clinical protocols that study the regulation and role of pulsatile gonadotropin-releasing hormone (GnRH) secretion. Studies include dynamic and repeated stimulation tests of pulsatile GnRH; plasma luteinizing hormone, follicular-stimulating hormone, testosterone (T), estradiol (E2), and GnRH measurements at cyclic and episodic intervals; and evaluation of adrenal androgen patterns. Circadian rhythms of GnRH secretion are monitored during sleep and awake hours. Growth hormone secretory patterns and responses to provocative stimuli are studied as clinically indicated. Selected participants undergo an assessment of pituitary responsiveness following T, E2, and/or naloxone infusions. The suppressive effects of E2 are also studied during the early follicular phase of the menstrual cycle. Endocrinologically normal children and normal adult men and women are also studied.

NCT00004335
Principal SponsorNational Center for Research Resources (NCRR)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 7 to 35 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Bone DiseasesBone Diseases, DevelopmentalBone Diseases, EndocrineBrain DiseasesCentral Nervous System DiseasesDwarfismGonadal DisordersHypopituitarismHypothalamic DiseasesMusculoskeletal DiseasesNervous System DiseasesPathologic ProcessesPituitary DiseasesPathological Conditions, Signs and SymptomsDisease AttributesDwarfism, PituitaryEndocrine System DiseasesHypogonadismPuberty, PrecociousRare Diseases

Criteria

PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Suspected or proven hypothalamic-pituitary-gonadal dysfunction, i.e.: Significant short stature and possible hypopituitarism Delayed adolescence Precocious puberty Isolated growth hormone deficiency (IGHD)Primary hypogonadism Women are also studied, including those with the following disorders: Infertility Oligo- or amenorrhea Hirsutism --Patient Characteristics-- Age: 7 to 16 (18 to 35 for women and volunteers) Other: No pregnant or nursing women No prisoners Not in neuropsychiatric institute or other facility for mental illness

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University of Michigan Health Systems

Ann Arbor, United StatesOpen University of Michigan Health Systems in Google Maps
CompletedOne Study Center