Health Medical

What Are the Risk Factors Associated with Clinical Trials?

After the COVID pandemic, we are seeing a variety of clinical trials news. Clinical trials are necessary for the medical industry and also for humanity. They help us get safe and effective medicines after comprehensive testing. Along with the positive aspects, there are some risk factors that every participant should understand. 

Clinical trials are nothing but experiments and there might be some things that could go wrong. If you are a participant or willing to participate in a trial, you must be aware of the risk factors associated with clinical trials

Clinical Trials and Associated Risks 

#1 – Side Effects 

One of the major risks associated with clinical trials is the side effects of the medicine. Because of this risk, the researchers take all precautions before administering the medicines to the participants. They obtain proper permission from the participants, administer small doses at first, monitor them, and then increase the doses. This ensures that none of the participants get adverse effects. 

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#2 – Procedural Reactions 

If the clinical trial involves a lot of medical procedures for better treatment of the participants, then it may cause certain adverse reactions. This is not a serious issue, but it is considered a risk. For example, patients who are undergoing regular X-rays or CT Scans might get radiation exposure, which is a minor risk for cancer development in future. Fortunately, the researchers take appropriate measures to avoid this issue. 

#3 – Emotional Risks 

This is quite common in clinical trials, as the participants are usually battling serious diseases. In such cases, they might get emotionally overwhelmed during the trial process. This can cause them to have emotional breakdowns, which can hinder the process of clinical trials. That’s why researchers take proper care of the participants and fulfil their psychological needs to avoid emotional stress buildup. 

#4 – Data Safety 

In the trials, the researchers collect a lot of data about the participants for better treatment. They collect personal data, including their family history, eating habits, medical history, and many other things. If there are any issues regarding the safe storage of the data, then it can get leaked, which is a major privacy risk for the participants. This is a serious ethical concern and causes various issues regarding the trials and personal lives of the participants. 

Final Words 

Experts and regulatory bodies deem clinical trials safe. However, as they are run by humans, we should not waive the chance of mishaps. In this post, we tried our best to cover all of the clinical trial risk factors. Anyone participating should be careful about these risk factors and get assurance from the researchers conducting the trials.