Actively Recruiting

Age: 18Years +
All Genders
NCT04543253

Recovery From Cushing Syndrome and Mild Autonomous Cortisol Secretion (MACS)

Led by Mayo Clinic · Updated on 2025-09-03

700

Participants Needed

1

Research Sites

592 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cushing syndrome (CS) is an endocrine disorder caused by chronic exposure to glucocorticoid (GC) excess. Endogenous CS has an estimated incidence of 0.2 to 5.0 cases per million per year and prevalence of 39 to 79 cases per million in various populations. CS usually affects young women, with a median age at diagnosis of 41.4 with a female-to-male ratio of 3:1. Following a curative surgery for CS, patients develop adrenal insufficiency and require GC replacement postoperatively until the hypothalamic-pituitary-adrenal (HPA) axis recovery occurs. Factors, such as age, gender, BMI, subtypes of CS, duration of symptoms, clinical and biochemical severity and postoperative GC dose have been reported to affect the HPA recovery in small retrospective studies. Glucocorticoid withdrawal syndrome (GWS) is a withdrawal reaction due to decrease in supraphysiological GC concentrations, which occurs after a successful surgery of CS. Glucocorticoid withdrawal syndrome (GWS) is under-recognized entity in patients undergoing curative surgery for endogenous Cushing syndrome. In this study we aim to determine pre- and post-surgical predictors of the duration and severity of glucocorticoid withdrawal in patients undergoing a curative surgery for cortisol excess and assess the effect of MUSE intervention on GWS severity in patients undergoing curative surgery for CS as compared to standard of care.

CONDITIONS

Official Title

Recovery From Cushing Syndrome and Mild Autonomous Cortisol Secretion (MACS)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 and above
  • New diagnosis of Cushing syndrome of any subtype (pituitary, adrenal, or ectopic) or mild autonomous cortisol secretion
  • Planning to undergo curative surgery
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Use of systemic supraphysiological glucocorticoids for more than 2 weeks within 1 month before enrollment
  • Unable to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Mayo Clinic

Rochester, Minnesota, United States, 55905

Actively Recruiting

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Research Team

V

Vanessa Fell, MA

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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