Using Doxepin for Urticaria
Sponsored by State University of New York - Upstate Medical University
About this trial
Last updated 3 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 2 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
- Between 18-65 years of age
- Presenting to Upstate Adult Emergency Department at either the Downtown or Community campuses.
- Diagnosed with isolated/acute urticaria
- Requires treatment with antihistamines to alleviate symptoms
Exclusion Criteria
- Pregnant women
- Prisoners
- Patients with altered mental status/have impaired decision-making capacity.
- Presenting with symptoms suggesting life threatening illness or anaphylaxis.
- Patients who have received any antihistamine (H1 antagonist) within the past 2 hours via any route of administration.
- Patients who have received an H2 antagonist within the past 2 hours.
- Patient received steroids by any route within the past 4 hours.
- Patient received epinephrine within the past 20 minutes.
- Patients currently taking concomitant p-glycoprotein inhibitors.
- Patients on any of the following CYP2D6 inhibitors: Bupropion, Fluoxetine, Paroxetine, Quinidine, Tipranavir.
- Patients with a history of serotonin syndrome.
- Patients currently taking another tricyclic antidepressant, selective serotonin reuptake inhibitor, and/or serotonin-norepinephrine reuptake inhibitor.
- Patients who have a condition where an antihistamine may be contraindicated.
- Patients with a contraindication to anticholinergic medications.
- History of adverse effects to tricyclic antidepressants or antihistamines.
- Patient who, based on their medical history or in the opinion of the clinician, have chronic urticaria, urticaria refractory to antihistamines, or dermatological disease that interferes with evaluation of a therapeutic response.
- Patients taking antileukotriene compounds (montelukast), calcineurin inhibitors (tacrolimus) or anti-serotonin agents (cyproheptadine)