Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Dundee
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
1. Mild to moderate stable asthmatics on ≤ 2000μg BDP or equivalent, who are methacholine responsive PC20\< 4 mg/ml
2. \>1dd change in methacholine PC20 after the administration of racemic Salbutamol.
3. Male or female 18-65
4. Informed Consent
5. Ability to comply with the requirements of the protocol
You may not be if
1. Severe asthmatics as defined by an FEV1≤ 60% or PEF variability \> 30% or with continual daytime or nocturnal symptoms.
2. The use of oral corticosteroids within the last 3 months.
3. Recent respiratory tract infection (2 months).
4. Significant concomitant respiratory disease such as COPD, CF, ABPA, bronchiectasis and active pulmonary tuberculosis.
5. Any other clinically significant medical condition such as unstable angina, acute myocardial infarction in the preceding 3 months, recent TIA/ CVA, that may endanger the health or safety of the participant, or jeopardise the protocol.
6. Any significant abnormal laboratory result as deemed by the investigators
7. Pregnancy, planned pregnancy or lactation
8. Known or suspected contra-indication to any of the IMP's
9. Concomitant use of medicines (prescribed, over the counter or herbal) that may interfere with the trial.
Clareo Health | Trough Bronchoprotection Conferred by Levosalbutamol and Racemic Salbutamol
