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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorMartin Blomberg Jensen

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Patients referred to or patients actively followed at the Department of Endocrinology and Internal Medicine at Herlev Hospital

Age 18-90

Disqualifiers

Lacking mental capacity to provide informed consent

Trial population

All patients referred or followed at the Department of Endocrinology and Internal Medicine, Herlev Hospital for suspected or confirmed: Osteoporosis, Hypercalcemia/PHPT, thyroid disease, adrenal disease, pituitary disease.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

20,000 Participants
are grouped into 5 trial groups
Group A: Patients with presumed osteoporosis
Group B: Patients with presumed Hypercalcemia / Primary Hyperparathyroidism
Group C: Patients with presumed thyroidal illness
Group D: Patients with presumed adrenal disease
Group E: Patients with presumed pituitary disease

Trial outcomes

Primary outcomes

1

Association between serum LH and hCG and risk of major osteoporotic fracture (MOF)

Among patients with suspected or confirmed osteoporosis

Time frame
From baseline up to 5-, 10-, and 15-year follow-up

Secondary outcomes

1

Association between serum LH and hCG and risk of later diagnosis of osteoporosis

Among patients with suspected or confirmed hypercalcemia/primary hyperparathyroidism

Time frame
From baseline up to 5-, 10-, and 15-year follow-up
2

Association between serum LH and hCG and urinary calcium/phosphate ratio

Among patients with suspected or confirmed hypercalcemia/primary hyperparathyroidism

Time frame
Baseline association
3

Association between serum LH and hCG and serum T4/T3 ratio

Among patients with suspected or confirmed thyroid disease

Time frame
Baseline association
4

Association between serum LH and hCG and risk of T3 treatment initiation

Among patients with suspected or confirmed thyroid disease

Time frame
From baseline up to 5-, 10-, and 15-year follow-up

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Martin Blomberg Jensen

Lead sponsor

Copenhagen University Hospital at Herlev

Sponsor institution

Copenhagen University Hospital at Herlev

Collaborator