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NCT04374721: CHROnOS
Clinical Study on Circadian Genes Dysregulation in Patients With Glucocorticoid Disorders
NA trial testing circadian gene expression evaluation in Cushing Syndrome in 44 participants. Status unknown.
1 June 2023
Quick facts
| Lead sponsor | University of Roma La Sapienza |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 44 |
| Start date | 4 July 2018 |
| Primary completion | 1 June 2023 |
| Estimated completion | 1 December 2023 |
| Sites | 1 location across Italy |
Drugs / interventions tested
- circadian gene expression evaluation
Conditions studied
- Cushing Syndrome — all drugs for Cushing Syndrome →
- Adrenal Insufficiency — all drugs for Adrenal Insufficiency →
- Cushing Disease — all drugs for Cushing Disease →
- Addison Disease — all drugs for Addison Disease →
Sponsor
University of Roma La Sapienza
Who can join
Adults 18 to 80, any sex, with Cushing Syndrome or Adrenal Insufficiency. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a multicentric, prospective, intervention study on circadian genes expression in peripheral blood mononuclear cells as biomarkers of circadian rhythm derangement in patients affected by alterations of endogenous glucocorticoids secretion (Cushing's Syndrome during active phase, treatment and under remission and newly or on established glucocorticoid replacement therapy adrenal insufficiency)
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Chronotherapy With Once-Daily Osilodrostat Improves Cortisol Rhythm, Quality of Life, and Sleep in Cushing's Syndrome.
Ferrari D, Bonaventura I, Simeoli C, Tomaselli A, et al · · 2025 · cited 18× · PMID 40172910 · DOI 10.1210/clinem/dgaf206 -
Circadian clock disruption impairs immune oscillation in chronic endogenous hypercortisolism: a multi-level analysis from a multicentre clinical trial.
Hasenmajer V, Sbardella E, Sciarra F, Simeoli C, et al · · 2024 · cited 12× · PMID 39612654 · DOI 10.1016/j.ebiom.2024.105462
Verify or expand the search:
- PubMed search for NCT04374721
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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- NCT05911620 — Evaluation of the Severity of Hepatic Fibrosis by Magnetic Resonance Elastography in the Diagnosis of Endogenous Hyperco · NA · recruiting
Other University of Roma La Sapienza trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04374721 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Roma La Sapienza
- Last refreshed: 30 November 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04374721.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing