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Completed No phase listed Observational

Study of the Prevalence of Endogenous Hypercortisolism in Patients With Resistant Hypertension (MOMENTUM)

ClinicalTrials.gov ID: NCT06829537

Public ClinicalTrials.gov record NCT06829537. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 2:11 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Study of the Prevalence of Endogenous Hypercortisolism in Patients With Resistant Hypertension in the United States of America (MOMENTUM)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a non-interventional study to assess the prevalence of endogenous hypercortisolism (eHC) in patients with resistant hypertension (rHTN) and will enroll approximately 1000 patients at approximately 45 sites in the United States (US). Each patient will have an initial visit for screening. After eligibility is confirmed, a limited exam will be performed and demographic and medical history will be collected. Non-fasting labs and a urine collection will also be done. A second visit will be a fasting blood draw at 8 AM after taking 1 mg of dexamethasone the night before at 11 PM. Cortisol level and study labs will also be collected. After the lab results are obtained, a third visit will be scheduled only for patients with eHC and will include a non-fasting blood draw at 8 AM and scheduling of a non-contrast CT scan.

Study identification

NCT ID
NCT06829537
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
1,143 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 28, 2025 (Actual)
Primary completion
Dec 8, 2025 (Actual)
Completion
Jan 23, 2026 (Actual)
Last update posted
Feb 17, 2026

2025 – 2026

United States locations

U.S. sites
50
U.S. states
15
U.S. cities
45
Facility City State ZIP Site status
Site 378 Huntington Park California 90255 —
Site 406 La Jolla California 92037 —
Site 538 La Jolla California 92037 —
Site 041 Los Angeles California 90048 —
Site 535 Northridge California 91324 —
Site 379 Redondo Beach California 90247 —
Site 542 Santa Maria California 93454 —
Site 387 Tarzana California 91356 —
Site 375 Torrance California 90502 —
Site 533 Torrance California 90505 —
Site 553 Cooper City Florida 33024 —
Site 444 Edgewater Florida 32132 —
Site 528 Maitland Florida 32751 —
Site 554 Miami Florida 33126 —
Site 525 Miami Florida 33155 —
Site 527 Miami Florida 33173 —
Site 537 Port Charlotte Florida 33952 —
Site 009 Atlanta Georgia 30303 —
Site 552 Chicago Illinois 60607 —
Site 532 Winfield Illinois 60190 —
Site 046 Covington Kentucky 41011 —
Site 061 Metairie Louisiana 70006 —
Site 377 New Orleans Louisiana 70112 —
Site 410 Baltimore Maryland 21239 —
Site 394 Olney Maryland 20832 —
Site 440 Rockville Maryland 20854 —
Site 067 Boston Massachusetts 02115 —
Site 530 Troy Michigan 48085 —
Site 371 Las Vegas Nevada 89148 —
Site 541 Reno Nevada 89502 —
Site 070 Albany New York 12203 —
Site 524 New York New York 10029 —
Site 181 Chapel Hill North Carolina 27514 —
Site 536 Durham North Carolina 27701 —
Site 555 Greenville North Carolina 27834 —
Site 529 Mooresville North Carolina 28117 —
Site 540 Morrisville North Carolina 27560 —
Site 059 Wilmington North Carolina 28401 —
Site 436 Cincinnati Ohio 45219 —
Site 551 Cleveland Ohio 44109 —
Site 042 Cleveland Ohio 44195 —
Site 195 Columbus Ohio 43201 —
Site 168 Charleston South Carolina 29425 —
Site 534 Mt. Pleasant South Carolina 29464 —
Site 456 Austin Texas 78759 —
Site 370 Dallas Texas 75230 —
Site 526 Houston Texas 77054 —
Site 408 Lufkin Texas 75904 —
Site 369 San Antonio Texas 78229 —
Site 531 Weslaco Texas 78596 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06829537, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 17, 2026 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06829537 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →