Adelaide Research Study Recruiting Participants With Asthma
Research Centre: CMAX Clinical Research
Location: 5/18a North Terrace, Adelaide SA 5000, Australia
Around 10% of the Australian population has a form of Asthma.
Studies are recruiting men & women between the ages of 18 & 55 with mild asthma. Participants will be receiving an investigational treatment that will be inhaled.
The study involves staying in-house for 12 days/nights (you cannot leave the site during this time) and 2 follow up visits. Participants will be paid after completion of the study.
- You may experience an improvement in your asthma symptoms.
- You will be helping to advance medical research.
- You will be contributing towards the development of a new asthma medication.
- You will be reimbursed for participating in this study.
- If you decide to participate in the study and later feel that you no longer wish to be part of it, you may withdraw at any time.
- Your records relating to this study and any other information received will be kept strictly confidential, except as required by the law.
- Qualified health professionals will monitor your health as it relates to the study.
Who Can Participate?
- Men and women aged 18-55 who suffer from mild asthma
- Able to stay 12 days/night in-house at the research site in Adelaide and attend 2 follow up visit appointments
What happens in a research study?
Each research study varies significantly, but there are some common elements. Most (but not all) studies involve taking a medication or undergoing some form of treatment. The patient or volunteer will first undergo screening to determine that they fit the medical eligibility criteria for the particular study, and then be given the study medication or treatment. The patient or volunteer typically returns to the research site a number of times to measure their response.
Are research studies safe?
Before trials are conducted on humans, new medications or treatments have usually undergone extensive examination in laboratories and are tried on cells and animals grown in labs. The ones with positive results are then approved for testing in human trials.
All research studies are conducted only after the approval of Ethics Committees and must follow the International Guidelines for Good Clinical Practice. Participation is always voluntary and a volunteer must read and agree to the Informed Consent document, which outlines what will happen in the study and all risks associated with participating. Participants can also ask questions to the medical staff, and of course can consult with their own Doctor. Volunteers also have the right to leave the clinical trial at any time.