Clinical trials involve recruiting participants for an experimental treatment. This provides valuable information that can be compared with current treatments. Outlined below are five reasons why it is beneficial to take part in clinical trials.
Research on the clinical trial for potential benefits
Before a clinical trial is conducted, healthcare professionals spend several years to gain knowledge on the proposed study. The trial will only be conducted if the information gathered shows that it would be beneficial.
Rigorous review by regulatory bodies
Clinical trials are reviewed by two bodies, namely the Research Ethics Committee (REC) and the Medicines and Healthcare products Regulatory Agency (MHRA) before they are performed. The Research Ethics Committee ensures that the clinical trial will be beneficial and cause minimal harm to volunteers. The Medicines and Healthcare products Regulatory Agency (MHRA) also ensures that medications used are safe for the public. These two bodies together make sure that the trial is safe and ethical before it is performed.
Well-trained clinical staff
During the trial, the participants are frequently monitored by clinical trial staff to ensure they are not being adversely affected. They are guided by trial protocols to ensure the safety of volunteers. Potential harm to participants is identified by staff during risk assessment. This enables them to look out for potential problems. In addition, the staff have also been trained on how to manage emergencies should they arise. In Adaptive Phase 1 Clinical Studies as performed by research teams such as those at http://www.richmondpharmacology.com, the trial design can be modified by the appropriate staff, where needed, to ensure that the volunteers are safe.
Benefit to general population
The information gathered from clinical trials at the end of the studies helps to determine if a treatment will be beneficial. The trial results can therefore positively influence how medicine is being practised and, in effect, the health of the community as a whole. Clinical trials need to have the right proportion of people; taking part in a trial can be a solution to that.
Incentive for all participants
Clinical trials usually involve two groups. One group receives the experimental medication whilst the other group, takes a placebo. The placebo does not contain the active ingredient. One might therefore not take the medication even if they are part of the trial. Everyone receives the same incentive regardless.