← Eichor
Study identifier: NCT07271485 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Propranolol for Misophonia

Condition: Misophonia · Propanolol · Misophonia Treatment  ·  Sponsor: Bloom Mental Health, LLC

PhaseEARLY_Phase 1
Planned participants20
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The primary goal of this study is to investigate whether a one-time dose of 20 mg oral propranolol can temporarily reduce the adverse emotional and physical symptoms triggered by misophonia. The secondary goals of this study are: 1. Determine potential predictors of response to propranolol treatment, including demographic factors, baseline symptom severity, psychometric instrument item responses, and physiological characteristics. 2. Evaluate the safety and tolerability of propranolol in individuals with misophonia.

This description comes directly from the study's public registry record.

Talk to the study team

Bloom Mental Health Clinic  ·  303-801-1776  ·  office@bloommh.com

Always discuss trial participation with your own doctor first.

Locations (1)

Bloom Mental HealthLittleton, Colorado, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07271485