Phase
Condition
Common Cold
Acute Rhinitis
Allergy
Treatment
N/AClinical Study ID
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female 18-70 years
Able to provide informed consent
Able to comply with the requirements of the protocol
Diagnosis of allergic rhinitis
Peak nasal inspiratory flow which is reversible to >20 l/min with oxymetazoline
Positive skin prick test to at least one common aeroallergen
Ability to withhold antihistamines, intranasal corticosteroids for duration of thestudy
Agreement for their GP to be made aware of study participation and to receive feedbackas relevant to the participant's well being
Exclusion
Exclusion Criteria:
Pregnancy, planned pregnancy or lactation
Respiratory tract infection in the previous 2 months
Nasal polyps of more than Grade I on nasal endoscopy
Any known adverse reaction to the Investigational Medicinal Product or otherquinazolines
Systolic BP <100mmHg
Any degree of heart block
Any clinically significant medical condition that may endanger the health or safety ofthe participant or jeopardise the protocol
Participation within another clinical trial of investigational medicinal productwithin the last 30 days
Under the age of 18
Benign hyperplasia, chronic urinary tract infections, bladder stones, overflowbladder, anuria or progressive renal failure
History of oesophageal or gastrointestinal obstruction or decreased lumen diameter ofthe gastrointestinal tract.
Concomitant use of PDE5 inhibitors (sildenafil etc.)
Alpha antagonists - this is the medication under investigation.
Other cardiovascular medications including but not limited to: ACE inhibitors, Angiotensin II antagonists, Beta blockers, calcium channel blockers,diuretics, nitrates, phosphodiesterase type-5 inhibitors or other vasodilating medications
these in combination with doxazosin carry an increased risk of symptomatic hypotension.
Monoamine oxidase inhibitors (MAOIs) - antidepressant medication that can lead tosignificant hypotension in combination with alpha antagonists.
Anxiolytics and hypnotics - enhanced hypotensive and sedative effects whenalpha-blockers given in combination with these.
Methyldopa and levodopa - potential enhanced hypotensive effect with alphaantagonists.
Nasal corticosteroid spray - would confound study outcomes
Oxymetazoline - this is used as an outcome of response in the study.
Antihistamines - the participants will be undergoing a histamine nasal challenge.
Sympathomimetics i.e. dopamine, ephedrine, epinephrine, metaraminol, methoxamine,phenylephrine- may reduce the effect of doxazosin.
Any other medication, which in the opinion of the Investigator may put the participantat risk.
Study Design
Connect with a study center
Brian Lipworth
Dundee, DD1 3AU
United KingdomSite Not Available

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