Clinical Trials Logo

Hypogonadism clinical trials

View clinical trials related to Hypogonadism.

Filter by:

NCT ID: NCT00080483 Completed - Hypogonadism Clinical Trials

Testosterone and Growth Hormone for Bone Loss in Men

Start date: March 2004
Phase: Phase 2
Study type: Interventional

Deficiency of testosterone, growth hormone, or both hormones can result in osteoporosis. If either hormone is replaced, the condition of the bones improves. The purpose of this study is to determine if dual hormone treatment for men deficient in testosterone and growth hormone improves bone structure more than testosterone treatment alone.

NCT ID: NCT00064987 Terminated - Hypogonadism Clinical Trials

Follicle Stimulating Hormone (FSH) to Improve Testicular Development in Men With Hypogonadism

Start date: April 2001
Phase: Phase 2
Study type: Interventional

Men with idiopathic hypogonadotropic hypogonadism (IHH, Kallmann Syndrome) may have small testicular size, low testosterone levels, no history of puberty, and infertility. These men lack a hormone called gonadotropin releasing hormone (GnRH) that stimulates the development and maturation of the testes. This study will investigate the impact of hormonal treatments on men with IHH. The goal of hormonal therapy is to maximize the potential fertility in these individuals.

NCT ID: NCT00048841 Completed - Prostate Cancer Clinical Trials

Prevention of Osteoporosis in Men With Prostate Cancer

Start date: May 2002
Phase: Phase 3
Study type: Interventional

The purpose of this two year study is to examine the safety and effectiveness of alendronate (Fosamax) for the prevention of bone loss in men with prostate cancer who are on therapy to lower their testosterone levels. All men will receive appropriate calcium and vitamin D supplements and one to two years of alendronate therapy. Bone density tests will be done every six months.

NCT ID: NCT00004438 Completed - Hypogonadism Clinical Trials

Leuprolide in Treating Adults With Hypogonadotropism

Start date: September 1997
Phase: N/A
Study type: Interventional

RATIONALE: Hypogonadotropism is an abnormal condition caused by decreased production of gonadotropins, a group of hormones that stimulate the parts of the reproductive system that produce and release eggs from the ovaries or sperm from the testicles. Leuprolide may stimulate the production of gonadotropins and be effective in increasing testosterone in men and inducing ovulation in women. PURPOSE: Clinical trial to study the effectiveness of leuprolide in treating adults who have hypogonadotropism.

NCT ID: NCT00004426 Completed - Hypogonadism Clinical Trials

Leuprolide in Determining the Cause of Gonadotropin Deficiency

Start date: August 1994
Phase: N/A
Study type: Interventional

RATIONALE: The body's response to one injection of leuprolide may provide more information than the standard test for gonadotropin deficiency in determining whether the cause of gonadotropin deficiency is related to the hypothalamus or the pituitary gland. PURPOSE: Randomized double-blinded clinical trial to study the effectiveness of leuprolide in determining the cause of gonadotropin deficiency.

NCT ID: NCT00004335 Completed - Hypogonadism Clinical Trials

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

Start date: April 1993
Phase: N/A
Study type: Observational

OBJECTIVES: I. Evaluate the sleep-entrained patterns of gonadotropin-releasing hormone (GnRH) and sex steroid secretion in normal and hypogonadal children. II. Examine the acute effects of sex steroids on the sleep-entrained patterns of GnRH secretion in pubertal children and normal adults, either by stimulation of endogenous production with pulsatile injection or by intravenous infusion of GnRH. III. Examine the role of endogenous opioids by means of opioid receptor blockade in the sex steroid regulation of GnRH secretion in pubertal children and normal adults.

NCT ID: NCT00001412 Completed - Hypogonadism Clinical Trials

Effects on the Brain of Lupron Induced Hypogonadotropic Hypogonadism With and Without Testosterone Replacement

Start date: December 1993
Phase: N/A
Study type: Observational

There is evidence that suggests male sex hormones (androgens) play a significant role in brain (central nervous system) functioning. In studies conducted with animals, researchers have documented that male sex hormones (androgens) are associated with neurotransmitter (serotonin) function, sexual behavior, aggression, and other non-reproductive behavior. Similar findings have been seen in studies involving humans. Androgens are thought to be involved in some neurologic conditions. Tourette's syndrome which is seen more often in males than females has caused researchers to look more closely at the effects of androgens on the brain. This study is designed to examine the effects of testosterone on brain (CNS) activity by first stopping testosterone release and then replacing it. Researchers will evaluate mood, behavior, cognitive (mental) function, physiologic response to serotonergic agonists and regional cerebral blood flow (r-CBF). This study will attempt to answer the following questions; 1. Is a person's mental functioning a result of being male or female (gender) or a result of the hormonal condition 3. Does the decrease of blood flow (r-CBF) to specific areas of the brain (prefrontal cortex) in women whose ovaries are not releasing hormones (hypogonadal state) also occur in men 4. Will the mental rotation task better identify hormone (gonadal steroid) differences in r-CBF 5. Do hormones directly influence the responsiveness of the hypothalamic-pituitary-adrenal (HPA) axis 6. Does the hormonal state of a patient directly affect levels of chemicals and steroids in the cerebrospinal fluid (CSF).

NCT ID: NCT00001275 Completed - Infertility Clinical Trials

Ovarian Follicle Function in Patients With Primary Ovarian Failure

Start date: May 12, 1991
Phase: N/A
Study type: Observational

No proven therapy to restore ovarian function and fertility is available to patients with karyotypically normal spontaneous premature ovarian failure. We know that one-half of these patients have primordial follicles remaining in the ovary, and these follicles can function intermittently. This is a diagnostic omnibus protocol that permits baseline clinical evaluation of patients with prematurem ovarian failure. The findings will determine patients' suitability for specifically focused therapeutic research protocols.