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NCT06578234: HYPER

Hyperemic mYocardial Perfusion by adEnosine at diffeRent Doses

Recruiting now Phase 4 Last updated 27 June 2025
What this trial tests

Phase 4 trial testing Adenosine in Chronic Coronary Syndrome in 180 participants. Currently enrolling.

Timeline
23 October 2024
Primary endpoint
31 December 2026
31 December 2026

Quick facts

Lead sponsorRegion Skane
PhasePhase 4
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposediagnostic
Enrollment180
Start date23 October 2024
Primary completion31 December 2026
Estimated completion31 December 2026
Sites1 location across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Region Skane — full company profile →

Who can join

40 and older, any sex, with Chronic Coronary Syndrome or Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Adenosine is a commonly used pharmaceutical stressor at cardiac magnetic resonance examinations to assess suspected chronic coronary syndrome (CCS). However, several studies have reported that the current use of adenosine does not induce adequate hyperemic response in a substantial number of patients, leading to false diagnostics. The aim of this trial is to investigate the hyperemic effect of the standard dose of adenosine (140 microgram/kg/min) to the high dose of adenosine (210 microgram/kg/min) to improve the diagnostic methods using adenosine as a stressor and ultimately improve treatment decisions and patient prognosis in CCS.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Adenosine

Trials testing the same drug.

Other recruiting trials for Chronic Coronary Syndrome

Currently open trials in the same condition.

Other Region Skane trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT06578234.

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