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More info
You can access this
clinical trial
if you have
Chronic Stable Angina or Periprocedural Myocardial Damage
and you are
between 18 and 75
years old
-
The phase for this study is not defined.
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The purpose

MYDA-MI study is a randomized, placebo controlled, double blind study performed in San Filippo Neri Hospital, Roma, Italy. The planned study duration is 18 months. The objectives are to assess the effects of pre-treatment with probiotic Ecoviesel on the incidence and magnitude of peri-procedural myocardial damage caused by coronary angioplasty in stable patients. 250 patients with chronic stable angina scheduled for a coronary angiography and possible ad hoc angioplasty will be randomized to receive pre-treatment with Ecoviesel sachets (each sachet contains 200 billions bacteria) or Placebo. The pre-treatment dosage will be 4 sachets of probiotic Ecoviesel or placebo for at least 2 weeks before the planned procedure. In patients undergoing angioplasty the same treatment will be continued for 4 weeks after PCI with secondary outcome measures performed at the end of this second stage.

Provided treatments

  • : Probiotic
  • Other: Placebo
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Locations near you

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Tris trial is registered with FDA with number: NCT02908776. The sponsor of the trial is San Filippo Neri General Hospital and it is looking for 250 volunteers for the current phase.
Official trial title:
Gut Flora Modulation for The Prevention of Pci-Related Myocardial Injury - A Randomized, Placebo Controlled, Double Blind, Investigator-Initiated, Single Centre, Preliminary Study