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OpenTrials
Completed

NCT Number: NCT03084562

Regadenoson vs Dipyridamole in Use as Pharmacological Stress Agent Before SPECT

Myocardial perfusion scintigraphy is to evaluate coronary perfusion as well as heart muscle function. This examination takes place in two stages, one imaging at rest and one after a cardiac stress caused. This stress can be triggered as a first-line stress test. A pharmacological stress is proposed when stress test is not possible or contraindicated, Several drugs have a marketing authorization in this indication (adenosine, dipyridamole, regadenoson, dobutamine).

Among them, the regadenoson is the most recent molecule. Marketed in France since 2013, it would allow a reduction of undesirable effects compared to other agents, especially adenosine. It is simple and quick to use thanks to a single dose administration. However, its cost is nearly 30 times higher than dipyridamole. In the investigational center, dipyridamole is currently the first-line pharmacological stress agent, whereas regadenoson is reserved for a limited number of doses, the indication of which must be justified (asthmatic patient or with severe COPD). Few studies in the literature specifically compare these two pharmacological agents (examination time, cost, tolerance) and the opinion on the use of regadenoson in the service is limited.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Lyon civil Hospital - Est Hospital Complexe - Nuclear Medicine Service

Bron, 69677, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult ≥ 18 years
  • Myocardial scintigraphy by pharmacological stress agent
  • Used molecules = Dipyridamole or Regadenoson

Exclusion criteria

  • Physical stress test by single or mixed effort (associating pharmacological stress)
  • Pharmacological agent used = Adenosine
  • Inclusion in the ERCAD protocol
  • Double isotope protocol
  • Patient refusal due to study information

Treatment and study plan

collect examination time, functional and clinical tolerability

Other

Examination time : time from patient setup and launch of the pre-test to the end of the patient monitoring Functional tolerability : functional assessed by the patient Clinical tolerability : clinical score by the cardiologist

Primary outcomes

  1. Duration of the test

    Time frame: 24 hours (Visit 1: During the examen)

    Evaluate the time savings from the use of regadenoson versus dipyridamole by comparing the duration of the test.

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Official study title

Descriptive Study Comparing Regadenoson Versus Dipyridamole in Use as Pharmacological Stress Agent Before a Myocardial Perfusion Imaging by Single Photon Emission Computed Tomography (SPECT)

Acronym: REDUCE

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Mar 21, 2017
Registry last updated
Apr 13, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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