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Clinical Trials in Denmark / NCT07824102
Recruiting Observational

Evaluation of the Role of Luteinizing Hormone (LH) and Human Chorionic Gonadotropin (hCG) in Adult Patients Undergoing Assessment for Endocrine Disorders

NCT07824102 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2026-01-01
Last updated
2026-09-17

Condition(s) studied

OsteoporosisHypercalcemiaPrimary HyperparathyroidismAdrenal Gland DiseasePituitary DiseaseThyroid Diseases

Study summary

Hormones are chemical messengers that help regulate many functions in the body. As women go through menopause, and as men age, levels of certain reproductive hormones change significantly. One of these hormones, luteinizing hormone (LH), increases substantially after menopause and may also rise in some men. Another hormone, human chorionic gonadotropin (hCG), is best known as the hormone of pregnancy, but small amounts can also be detected in some postmenopausal women and older men.

Recent research suggests that LH and hCG may have effects beyond reproduction. These hormones may influence bone health, body weight, kidney function, thyroid function, and adrenal gland function. However, little is known about their importance in patients with endocrine disorders.

The purpose of this study is to investigate whether blood levels of LH and hCG are associated with the presence, severity, and long-term outcomes of endocrine diseases. The study will include adult patients undergoing evaluation for hormonal disorders. Blood samples will be analyzed for LH, hCG, and other relevant hormones and biomarkers. Participants will also be followed through national health registries to examine whether these hormone levels are associated with future health outcomes.

The results of this study may improve our understanding of how LH and hCG affect the body and help determine whether these hormones can be used as biomarkers to improve the diagnosis and management of endocrine diseases.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Patients referred to or patients actively followed at the Department of Endocrinology and Internal Medicine at Herlev Hospital * Age 18-90 Exclusion Criteria: * Lacking mental capacity to provide informed consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Endocrinology and Internal Medicine, Herlev Hospital Herlev Denmark Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07824102 on ClinicalTrials.gov ↗ ← All trials in Denmark