Assessment of Emergency Spacers Versus Traditional Spacers for Delivery of Aerosolized Drugs

Recruiting Phase 4 Interventional Study
Asthmatic Patients MDI Aerosol Generating Procedure
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
6 – 80
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Other
Participants needed
120 (estimated)
Sponsor
Beni-Suef University · Other
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About This Trial
* The goal of this clinical trial is to evaluate the performance, feasibility, and safety of emergency spacers compared to traditional spacers for the delivery of aerosolized drugs using pMDI. in young children and adult asthmatic patients The main questions it aims to answer are: 1. Measuring total emitted dose emitted from pMDI alone and attached to spacers. 2. Determining the pharmacokinet…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: • Mild and moderate asthmatic patients aged from 6 - 80 year old. Exclusion Criteria: * Severe asthmatics or patients admitted to an intensive care unit * ischemic heart disease * recent abdominal surgery * inability to perform properly the pulmonary function tests * hepatic o…
Contacts

Omar Ahmed Sayed, Demonstrator

+201152677683

OmarAhmed@pharm.bsu.edu.eg

CONTACT

Omar Ahmed Sayed, Demonstrator

+201090313474

omarahmedsayed1111@gmail.com

CONTACT