Endocrine Disease

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Review clinical trials related to Endocrine Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Study of Endocrine-Related Conditions and Physiology

Background: Endocrine disorders involve changes to glands that produce hormones. Hormones are released by these glands into the blood so they can direct the function of other tissues in the body. Researchers want to study people who may have endocrine disorders. They want to learn more about the conditions that affect endocrine glands. Objective: To study adults with a variety of endocrine disorders for research and physician education. Eligibility: Adults ages 18 and older who have an endocrine or metabolic-related disorder Healthy volunteers 18 and older Design: Participants will be screened with a review of their medical records. Participants will have a physical exam and medical history. The length of the study and the schedule will vary by participant. Tests may include: Blood and urine tests Stool and saliva samples Imaging studies: Participants will lie on a table while a machine takes pictures of the body. They may be injected with a substance to make their organs more visible in the pictures. Tests of endocrine tissue function Consultation with other specialists Sleep study Medical photographs Participants may be treated for their endocrine disorder. This could include: Surgery. If tissue is removed during surgery, it may be studied. Radiation Medicine Participants may have genetic testing. This will be done with a small amount of blood, cells from a cheek swab, or saliva. Sponsoring Institution: National Institute of Digestive, Diabetes and Kidney Disease ...

Participants needed: 1,000
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Updated: Oct 13, 2026Locations: 1
Eligibility criteria

Adult men and women age 18 years or older. [+2]

Unstable participants and participants with severe organ failure, or those with... [+2]

Status: Recruiting

Diagnosis of Pheochromocytoma

The goal of this study is to develop better methods of diagnosis, localization, and treatment for pheochromocytomas. These tumors, which usually arise from the adrenal glands, are often difficult to detect with current methods. Pheochromocytomas release chemicals called catecholamines, causing high blood pressure. Undetected, the tumors can lead to severe medical consequences, including stroke, heart attack and sudden death, in situations that would normally pose little or no risk, such as surgery, general anesthesia or childbirth. Patients with pheochromocytoma may be eligible for this study. Candidates will be screened with a medical history and physical examination, electrocardiogram, and blood and urine tests. Study participants will undergo blood, urine, and imaging tests, described below, to detect pheochromocytoma. If a tumor is found, the patient will be offered surgery. If surgery is not feasible (for example, if there are multiple tumors that cannot be removed), evaluations will continue in follow-up visits. If the tumor cannot be found, the patient will be offered medical treatment and efforts to detect the tumor will continue. Main diagnostic and research tests may include the following: 1. Blood tests - mainly measurements of plasma or urine catecholamines and metanephrines as well as methoxytyramine. If necessary the clonidine suppression test can be carried out. 2. Standard imaging tests - Non-investigational imaging tests include computed tomography (CT), magnetic resonance imaging (MRI), sonography, and 123I-MIBG scintigraphy and FDG (positron emission tomography) PET/CT. These scans may be done before and/or after surgical removal of pheochromocytoma. 3. Research PET scanning is done using an injection of radioactive compounds. Patients may undergo 18F-FDOPA, 18F-DA, as well as 68Ga-DOTATATE PET/CT . Each scan takes up to about 2 hours. 4. Genetic testing - A small blood sample is collected for DNA analysis and other analyses.

Participants needed: 3,000
Trial details
Phase: Phase 1Age: 3-120Biological sex: AllType: InterventionalSponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Updated: Oct 8, 2026Locations: 1
Eligibility criteria

High levels of blood or urinary catecholamines, metanephrines, methoxytyramine o... [+5]

Pregnant or breastfeeding women [+12]

Status: Not yet recruiting

Exhaled Breath Electronic Nose for Multi-Disease Risk Prescreening

This prospective multicenter observational study will evaluate whether an electronic nose that analyzes patterns in exhaled breath can be developed as a noninvasive tool for early risk prescreening across several disease areas. The study will enroll up to 20,000 adults from hospitals and health examination centers. It will first establish a standardized breath-sampling and quality-control procedure and assess repeatability across breathing maneuvers, devices, centers, and time. It will then develop and independently evaluate risk prescreening models for prespecified disease modules, including lung cancer/clinically significant pulmonary nodules, chronic respiratory diseases, and metabolic/endocrine diseases, with additional exploratory modules involving liver, kidney, cardiovascular, and systemic inflammatory/infectious/immune conditions. The electronic-nose results are for research only and will not be reported to participants or clinicians or used to change routine screening, diagnosis, or treatment. Disease reference status will be determined from examinations, laboratory tests, imaging, pathology, pulmonary function testing, specialist assessments, or follow-up that are already performed as part of routine care. The study will evaluate screening sensitivity, specificity, false-negative rate, predictive values, calibration, and performance across different centers, devices, and time periods.

Participants needed: 20,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: The First Affiliated Hospital of Guangzhou Medical UniversityUpdated: Sep 4, 2026Duration: 2 Years
Eligibility criteria

Not listed

Status: Not yet recruiting

Anticipated Stigma, Illness Identity, and Quality of Life in Male Hypogonadism

This study aims to systematically compare the levels of anticipated illness stigma and illness identity among men diagnosed with hypogonadism to those of men with other chronic endocrine conditions (e.g., diabetes mellitus, hypothyroidism, and hypertension). Furthermore, it examines whether these psychosocial variables predict quality-of-life deterioration specifically within the hypogonadism cohort.

Participants needed: 90
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Hacettepe UniversityUpdated: Aug 7, 2026Locations: 2Duration: 1 Day
Eligibility criteria

Male, aged 18 years or older. [+10]

Active psychiatric diagnosis (e.g., active psychosis, bipolar disorder). [+6]

Status: Recruiting

Environment, Inflammation and Metabolic Diseases Study

The aim is to establish an effective and practical early warning model for endocrine and metabolic diseases based on an environmental-gene-protein panoramic network, to uncover new mechanisms underlying the onset and progression of these diseases, and to screen for novel therapeutic targets.

Participants needed: 8,000
Trial details
Biological sex: AllType: ObservationalSponsor: Qifu LiUpdated: Apr 6, 2026Locations: 1Duration: 5 Years
Eligibility criteria

All individuals who voluntarily participated in the physical examination

Status: Recruiting

New Clinical Decision Support Score Based on Steroid Hormone Profiling in the Diagnosis of MACS

The recent development of quantitative steroid metabolome profiling could be of interest for the positive diagnosis of mild autonomous cortisol-secreting adenoma (MACS). The aim of the study is to develop a predictive model of MACS status or non-secreting adenoma (NSA) based on a panel of 19 serum steroids and three clinico-biological parameters (body mass index or BMI, fasting glycaemia, blood pressure) and to estimate its performance for the diagnosis of MACS in a cohort of patients followed in the endocrinology department of Bordeaux University Hospital.

Participants needed: 291
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, BordeauxUpdated: Jan 20, 2026Locations: 1
Eligibility criteria

18 years ≤ Age [+15]

Status: Recruiting

Comprehensive Data Collection and Follow-Up for Patients With Thyroid, Parathyroid and Adrenal Disease

The goal of this data review study is to collect data to learn more about thyroid, parathyroid, and adrenal disease.

Participants needed: 15,000
Trial details
Biological sex: AllType: ObservationalSponsor: M.D. Anderson Cancer CenterUpdated: Sep 17, 2019Locations: 1
Eligibility criteria

All patients that are being seen at MD Anderson with diagnosed or suspected endo... [+1]