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Using Doxepin for Urticaria

The Use of Doxepin for Urticaria in the Emergency Department

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05115136
Enrollment
160
Registered
2021-11-10
Start date
2022-05-23
Completion date
2023-07-01
Last updated
2022-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urticaria

Brief summary

Isolated urticaria in the emergency department is widely treated by physicians with histamine blocking agents such as diphenhydramine, cetirizine, and cimetidine. Doxepin is a tricyclic antidepressant that has been shown to have much higher concentrations of histamine blocking activity and therefore may be useful in treating urticaria. The purpose of this study is to compare the effectiveness of using doxepin verses a traditional medication, diphenhydramine (Benadryl), in the treatment of isolated urticaria in the emergency department.

Interventions

25mg dose of Doxepin will be administered one time, by mouth

DRUGDiphenhydramine

50 mg dose of Diphenhydramine will be administered one time, by mouth

Sponsors

State University of New York - Upstate Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Improvement of urticaria1 hour after med administration, 2 hours after administration, and prior to discharge.Improvement of urticaria based on pruritis score. Scale is from 1-5, lower the score the better.

Countries

United States

Contacts

Primary ContactDavid Andonian, MD
andoniad@upstate.edu315-464-4363

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026