Overview

Effect of Midazolam and Dexmedetomidine on Heart Function - A Randomized MRI-based Study.

Status:
Completed
Trial end date:
2019-12-31
Target enrollment:
0
Participant gender:
All
Summary
To compare the changes in heart function, induced after sedation with midazolam or dexmedetomidine, using cardiac magnetic resonance imaging (MRI). This study is a randomized unmasked study, in which participant will be allocated by the envelop method into the dexmedetomidine (DEX) group or into the midazolam (MID) group.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Masaryk Hospital Krajská zdravotní a.s.
Treatments:
Dexmedetomidine
Midazolam
Criteria
Inclusion Criteria:

- Patients who were admitted due to chest pain, in whom acute coronary syndrome,
pulmonary embolism and acute aortic syndrome were ruled out

- Age ≥18 and ≤ 65 years

- No contraindication to provide cardiac MRI

- No known allergy to Midazolam or Dexmedetomidine

- Signed informed consent

- No history of heart, hepatic, renal or respiratory failure

Exclusion Criteria:

- Atrial fibrilation

- Claustrophobia

- Heart Failure

- Renal Failure

- Hepatic disease

- Respiratory insufficiency

- Fertility and lactation

- Patients who cannot cooperate or refuse to sign the consent.