OBServation of Environment and ReproductiVe Endocrine Effects Study (OBSERVE Study)

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Background: Endocrine disorders occur when the glands that make hormones do not work properly. Hormones levels that are too high or too low can cause problems such as late or early puberty, irregular periods, and infertility. Environmental factors - including pollution; chemical exposure at home and work; foods; medicines; and sleep habits - may cause problems with the endocrine and reproductive systems.

Objective: To learn how environmental factors may affect the endocrine and reproductive systems.

Eligibility: Males or females, referring to sex assigned at birth, aged 8 years and older; they must have hypogonadism, infertility, or other reproductive disorders.

Design: Adult participants will have 4 to 5 visits in 5 years. Children may have up to 12 visits; they may remain in the study up to the age of 23. Most visits will be less than 3 hours. Participants will be screened. They will have a physical exam. They will have blood and urine tests. They will complete questionnaires; they will answer questions about their diet, health, and other topics. Some may be referred for additional tests, such as imaging scans and semen analysis. Specific tests conducted during study visits will vary, depending on the participant s diagnosis. In addition to repeated blood and urine tests, these may include: Body composition measure: Participants will sit in a pod-shaped machine for about 6 minutes. The machines measures the air inside the capsule to record body fat and breathing volume. Resting energy expenditure test: Participants will lie down with a clear dome placed over their head. They will breathe quietly for 30 minutes. This test measures the number of calories their body burns at rest. ...

Eligibility
Participation Requirements
Sex: All
Minimum Age: 8
Maximum Age: 99
Healthy Volunteers: f
View:

• In order to be eligible to participate in this study, an individual must meet all of the following criteria:

• Male or female, referring to sex assigned at birth (cis gender)

• Age \> 8 years and weight \>= 12 kg

• A diagnosis of hypogonadism, infertility or other reproductive dysfunction

• Some specific diagnoses (as defined in standard guidelines) will include:

⁃ Male or female hypogonadism

∙ Obesity/metabolic syndrome related to hypogonadism.

‣ Other reproductive dysfunction (e.g., secondary to endocrine dysfunction, thyroid disorders, Cushing syndrome, pharmacotherapy, etc.)

‣ Premature Ovarian Insufficiency

‣ Isolated hypogonadotropic hypogonadism

⁃ Polycystic Ovarian Syndrome

⁃ Delayed Puberty

⁃ Precocious puberty

⁃ Perimenopause and post-menopausal states

⁃ Androgen Excess States (Nonclassic Congenital Adrenal Hyperplasia, Extreme hyperinsulism, Idiopathic etc.)

• or

⁃ Exhibiting signs of a diagnosis of hypogonadism, e.g., Bosma arrhinia microphthalmia syndrome (BAMS)

• Ability of participant, legal guardian, or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.

Locations
United States
North Carolina
NIEHS Clinical Research Unit (CRU)
RECRUITING
Research Triangle Park
Contact Information
Primary
NIEHS Join A Study Recruitment Group
myniehs@nih.gov
(855) 696-4347
Backup
Natalie D Shaw, M.D.
natalie.shaw@nih.gov
(984) 287-3716
Time Frame
Start Date: 2024-07-01
Estimated Completion Date: 2039-03-31
Participants
Target number of participants: 300
Treatments
Androgen Excess States
Polycystic Ovary Syndrome (PCOS);Women who meet criteria for PCOS based on NIH/ Rotterdam or other clinical criteria
Congenital Adrenal Hyperplasia / Hyperandrogenism
Women who exhibit evidence of hyperandrogenism not related to Polycystic Ovarian Syndrome (PCOS); Nonclassic Congenital Adrenal Hyperplasia, Extreme hyperinsulism, Idiopathic etc.
Exhibiting signs of a diagnosis of hypogonadism
for example: Bosma arrhinia microphthalmia syndrome (BAMS)
Hypogonadism / Infertility
Isolated hypogonadotropic hypogonadism
Hypothalamic Amenorrhea (HA) (female) Functional Hypogonadism (male)
Participants who experience secondary or primary amenorrhea, or male hypogonadism, in the setting of negative energy balance such dieting, eating disorders or exercise training
Miscellaneous
Reproductive disorders not related to the above categories. (e.g., secondary to endocrine dysfunction, thyroid disorders, Cushing syndrome, pharmacotherapy, etc.)
Precocious or Delayed Puberty
Participants who display clinical evidence of delayed or precocious puberty based on standard criteria.
Premature Ovarian InsufficiencyPerimenopause or post-menopausal states
Women who attain menopause before age 40 years (or as defined by clinical criteria). Perimenopausal women are those typically above age 40 years and experience secondary amenorrhea/ oligomenorrhea.
Weight *Overweight/Underweight
BMI below or above reference standard (Adult Reference: Asians/ Asian Americans- 18.5-22.9 kg/m2; Other races- 18.5-24.9 kg/m2\*Participants may simultaneously belong to cohort of weight and any other cohort.
Sponsors
Leads: National Institute of Environmental Health Sciences (NIEHS)

This content was sourced from clinicaltrials.gov