Center for Clinical Pharmacology
Leuven, 3000, Belgium
NCT Number: NCT04399148
In order to validate the accuracy and reliability of the histamine skin prick model for histaminergic itch and vasodilation, the dermal blood flow response induced by a histamine skin prick will be evaluated after the administration of certain antipruritics. Besides, the influence of these antipruritics on the dermal blood flow response induced by the topical application of cinnamaldehyde and capsaicin will be evaluated. Changes in dermal blood flow will be measured with laser speckle contrast imaging.
Looking for future studies?
Notify Me18 year–45 year
Male
Interventional
Not applicable
Leuven, 3000, Belgium
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Desloratadine (H1-antihistamine): oral tablet (1 x 5 mg), taken with 240 ml water, 4 hours prior to the histamine skin prick
Aprepitant (NK1-antagonist): hard capsule (1 x 125 mg), taken with 240 ml water, 4 hours prior to the histamine skin prick
Ketotifen (H1-antihistamine and mast cell stabilizer): capsule (1 x 1 mg), taken with 240 ml water, 4 hours prior to the histamine skin prick
Time frame: The dermal blood flow will be assessed before (baseline) and every 10 minutes during the hour following the skin pricks
Time frame: The dermal blood flow will be assessed before (baseline) and every 10 minutes during the hour following application
Universitaire Ziekenhuizen KU Leuven
Other
Influence of Antipruritics on the Dermal Blood Flow Response After a Histamine Skin Prick as Well as After the Topical Application of Cinnamaldehyde and Capsaicin
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04950127
Bile Duct Diseases, Biliary Tract Diseases
Erlangen, Germany
View Trial DetailsNCT07641530
Hemodialysis, Pathological Conditions, Signs and Symptoms
Izmir, Turkey (Türkiye)
View Trial DetailsNCT06800755
Dry Skin, Pathological Conditions, Signs and Symptoms
Gdansk, Poland
View Trial DetailsNCT07478133
Pathological Conditions, Signs and Symptoms, Pruritus
Wuxi, Jiangsu, China
View Trial Details