Atomoxetine for Fainting (Vasovagal Syncope)
(POST7 Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests atomoxetine, a medication, to determine if it can prevent fainting spells in individuals with recurrent vasovagal syncope, a condition causing sudden drops in heart rate and blood pressure that lead to fainting. The goal is to find a simple treatment to reduce fainting incidents and improve the quality of life for those affected. Participants will receive either atomoxetine or a placebo (a harmless pill with no active drug) to compare results. Individuals who have fainted at least twice in the past year due to vasovagal syncope might be suitable for this study. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to a potentially groundbreaking treatment.
Will I have to stop taking my current medications?
Yes, you will need to stop taking certain medications before participating in this trial. Specifically, you cannot be on β-blockers, bupropion, α1-adrenergic agonists or antagonists, tricyclic antidepressants, serotonin reuptake inhibitors, scopolamine, theophylline, or fludrocortisone.
Is there any evidence suggesting that this treatment is likely to be safe for humans?
Research shows that atomoxetine, a drug approved for treating attention deficit disorder, is being tested for its potential to help with vasovagal syncope, a type of fainting spell. In earlier studies, participants who took atomoxetine fainted less often than those who received a placebo. Specifically, one study found that fewer participants fainted during a tilt test after taking atomoxetine compared to a placebo (10 out of 29 with atomoxetine vs. 19 out of 27 with placebo).
Regarding safety, atomoxetine is generally well-tolerated. Since the FDA has already approved it for another use, extensive safety information is available. However, like any medication, it can have side effects. Prospective clinical trial participants should discuss these potential side effects with their healthcare provider to make an informed decision.12345Why do researchers think this study treatment might be promising for fainting?
Unlike the standard treatments for vasovagal syncope, which often include lifestyle changes and medications like beta-blockers or fludrocortisone, atomoxetine offers a unique approach. Atomoxetine is traditionally used for ADHD and works by increasing norepinephrine levels, which may help stabilize blood pressure and reduce fainting episodes. This new mechanism of action is what excites researchers, as it targets the condition from a different angle, potentially offering relief for those who don't respond well to existing therapies.
What evidence suggests that atomoxetine might be an effective treatment for vasovagal syncope?
Research has shown that atomoxetine, a medication typically used for attention deficit disorder, might help reduce fainting episodes in people with vasovagal syncope. In this trial, participants will receive either atomoxetine or a placebo. One study found that fewer people fainted when taking atomoxetine compared to those taking a placebo. Specifically, only 10 out of 29 people fainted on atomoxetine, while 19 out of 27 fainted on the placebo. Another study found that 11 out of 12 people improved with atomoxetine, and 7 of them did not faint at all. These results suggest that atomoxetine may help prevent fainting by affecting a part of the body that controls reflexes related to fainting. This makes atomoxetine a possible treatment for those who often experience troublesome fainting spells.56789
Are You a Good Fit for This Trial?
This trial is for adults who've fainted at least twice in the past year due to vasovagal syncope, as defined by American College of Cardiology Guidelines. Participants must be over 18 and score at least -2 on a specific Syncope Symptom Score. Those with uncontrolled blood pressure or thyroid issues, pacemakers, certain eye conditions, or taking conflicting medications cannot join.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants are randomized to receive either atomoxetine 40 mg twice daily or matching placebo in a double-blind, crossover trial
Follow-up
Participants are monitored for safety and effectiveness after treatment
Extension
Optional open-label extension for continued monitoring and assessment of long-term effects
What Are the Treatments Tested in This Trial?
Interventions
- Atomoxetine Hydrochloride
Atomoxetine Hydrochloride is already approved in United States, European Union, Canada for the following indications:
- Attention Deficit Hyperactivity Disorder (ADHD)
- Attention Deficit Hyperactivity Disorder (ADHD)
- Attention Deficit Hyperactivity Disorder (ADHD)
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Calgary
Lead Sponsor