Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
PATH
Age
18–55
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Female and male participants ages 18 to 55 years.
Healthy enough to participate in the clinical trial per site investigator assessment.
Healthy skin on the upper deltoid region of both arms.
Able to provide signed informed consent and understand study procedures per ICH/GCP guidelines.
Literate in English.
Available by telephone 48 hours after the study visit.
You may not be if
Skin abnormalities on upper deltoid region of either arm (scars, rash, infection) or other skin conditions that would interfere with the ability to visualize an intradermal injection in the opinion of the investigator.
Unable to understand the study purpose or procedures.
Clareo Health | Performance and Safety Evaluation of an Intradermal Delivery Device