ClinicalTrials.gg
RecruitingNCT03867448Updated Oct 26, 2026

Study of Endocrine-Related Conditions and Physiology

An observational study in Endocrine Disease, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). Recruiting at 1 site in United States. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · Observational

From the registry’s dates

  • Started Mar 2019; still recruiting 7 years 7 months later.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
1,000
Ages
18 Years to 90 Years
Sex
All
01

Study summary

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

Read the detailed description

Study Description:

This study allows the NIH Intramural Endocrinology Training Program (IETP) to follow or provide evaluation, treatment and or interventions to certain eligible subjects.

Objectives:

  1. To provide a repository of data and samples obtained during the course of clinical care to allow for future research.
  2. To add value to the IEFP training program by maintaining a diverse group of endocrine conditions seen at the NIH.
  3. To provide a vehicle by which pilot studies of endocrine physiology can be initiated.
  4. To identify prismatic cases that deviate from known presentations or responses to treatment.
  5. To evaluate the safety and results from adrenal venous sampling using a modified catheter with side hole placement.

Endpoints:

  1. Data from standard of care evaluation and management.
  2. Adverse events during and after adrenal vein sampling; cortisol and aldosterone results from the sampling.
02

Conditions studied

  • Endocrine Disease

Keywords

  • Adrenal Gland
  • Pituitary
  • Natural History
03

In context

Endocrine System Diseases

322 studies on the registry are indexed under Endocrine System Diseases; 51 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 134 across 88 observational studies indexed under Endocrine System Diseases.

Browse Endocrine System Diseases studies →

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) is the lead sponsor of 538 studies on the registry; 55 are open to participants now.

Of its 80 completed or terminated interventional studies of FDA-regulated products, 51 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

any adult with a potential endocrine disorder; the types of disorders may vary to ensure that there is an adequate case mix of diagnoses for the training program.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

  • Adult men and women age 18 years or older.
  • Known or suspected endocrine disorders requiring clinical screening, management and/or treatment and follow-up.
  • Stated willingness to comply with all study procedures and availability for the duration of the study

Exclusion criteria

EXCLUSION CRITERIA:

  • Unstable participants and participants with severe organ failure, or those with a condition or medical treatment that may affect/limit the endocrine work-up and exhaust Clinical Center, IETP resources will be excluded if appropriate.
  • Inability of a subject to adhere to a proposed schedule of visits.
  • Inability to provide .
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
1,000 participants (estimated)

Groups and cohorts

  • Adults with Endocrine Disorder

    Adults referred to NIH with possible endocrine conditions

  • Adults with hyperaldosteronism

    Adults referred to NIH or studied at NIH and determined to have hyperaldosteronism

    Device: Creation of side holes in catheters for adrenal vein sampling

Interventions

  • DeviceCreation of side holes in catheters for adrenal vein sampling

    one or two side-holes will be created by the interventional radiologist to facilitate adrenal vein sampling

06

What researchers measure

Primary outcomes

  1. Diagnosis/Treatment

    determination of diagnosis and/or treatment of an endocrine disorder

    Time frame: variable

07

Study locations

1 of 1 sites recruiting
  • National Institutes of Health Clinical Center
    Bethesda, Maryland 20892, United States
    Recruiting
    • For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) · Contactprpl@cc.nih.gov · 800-411-1222
08

References and documents

Individual participant data

Plan to share: Undecided — WE currently have no plan to share this data, but in the future may consider sharing of this data for analysis with collaborators of with other expertise.

09

Timeline

4 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Mar 2019 (actual). Primary completion is estimated for Jan 2036, 201 months after the start.

Of 32 observational studies under Endocrine System Diseases, half reached primary completion within 43 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 339. This study's planned 201 months is above that.

Endocrine System Diseases covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 7, 2019
First posted
Mar 8, 2019
StartActual
Mar 27, 2019
Primary completionEst.
Jan 1, 2036
CompletionEst.
Jan 1, 2036
Last update
Oct 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: description
4 updates, last Oct 26, 2026
Show all 4 updates
  1. Oct 26, 2026
    Minor edits only
    + 1 other change: description
  2. Oct 13, 2026
    Minor edits only
    + 1 other change: description
  3. Oct 2, 2026
    Minor edits only
    + 1 other change: description
  4. Sep 28, 2026
    Minor edits only
    + 1 other change: description

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT03867448
Responsible party
Sponsor
First posted
Mar 8, 2019
Start date
Mar 27, 2019
Primary completion
Jan 1, 2036 (estimated)
Completion
Jan 1, 2036 (estimated)
Last update
Oct 26, 2026

Study contacts

Raven N McGlotten, R.N.
Contact
mcglottenr@mail.nih.gov
(301) 827-0190
Lynnette K Nieman, M.D.
Contact
niemanl@mail.nih.gov
(301) 496-8935
Lynnette K Nieman, M.D.
principal investigator · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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