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Metanephrines in Obstructive Sleep Apnoea

Utility of Plasma and Urine Metanephrines in the Diagnosis of Phaeochromocytoma in Patients With Obstructive Sleep Apnoea

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05053685
Enrollment
81
Registered
2021-09-22
Start date
2020-07-29
Completion date
2023-08-29
Last updated
2024-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Catecholamine; Secretion, Obstructive Sleep Apnea, Pheochromocytoma

Brief summary

Although most patients have essential (unexplained) hypertension, some patients have a treatable underlying condition. One such condition is phaeochromocytoma, a tumour that produces excessive stress hormones. Left undiagnosed, patients may develop a hypertensive crisis that can be fatal. Measurements of stress hormones (both 24-hour urine collection and morning blood tests) are highly sensitive for detecting these tumours. However, these stress hormones may also be elevated in obstructive sleep apnoea (OSA) which affects 1 in 5 adults. The investigators hypothesize that in patients with OSA, blood tests will be better than 24-hr urine tests at ruling out a tumour. If this is confirmed, then OSA patients with suspected phaeochromocytoma could be investigated with a morning blood test instead of a traditional urine test, reducing unnecessary additional tests and patient anxiety. In this single site study, the investigators plan to recruit 70 patients undergoing polysomnography. 24hr urine and bloods will be measured. Patients with elevated hormone levels will undergo imaging to rule out a tumour. The primary outcome will be the accuracy of each test in ruling out a tumour. The secondary outcomes will be the relationship between stress hormone level and severity of OSA, which may help to explain the increased cardiovascular risk in patients with OSA, and the change in stress hormone level with treatment for OSA

Interventions

DIAGNOSTIC_TESTMeasurement of Urine and plasma metanephrines

Measurement of Urine and plasma metanephrines

Sponsors

Changi General Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients aged 21-70 years attending for a sleep study to evaluate for OSA

Exclusion criteria

* Medications that can cause changes in metanephrine levels * Other factors that can cause changes in metanephrine levels * Renal impairment (eGFR \< 60ml/min) * Other serious medical conditions

Design outcomes

Primary

MeasureTime frameDescription
Urine and plasma metanephrines1 yearMeasurement of 24 hours urine metanephrines

Secondary

MeasureTime frameDescription
Relationship between metanephrine level and severity of OSA1 yearcomparison of metanephrine level and severity of OSA as dertermined by sleep study
Change in metanephrine levels with treatment for OSA1 yearChange in plasma and urine metanephrine levels during treatment for OSA

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026