Essay on the Treatment of Clinical Trials Participants
Clinical trials are research studies which aim to discover different treatment options and make sure that they are safe and effective to be used. Such trials also add to the knowledge and information regarding medical and provide with the relevant data which can help make effective decisions of health care. It is important to ensure the safety of the participant as well by reducing the unsatisfactory or harmful side effects of tests for different small groups.
The process of clinical trials mainly has four phases which focus on the treatment, screening, diagnostic, prevention, health service, research, supportive care, and basic science. Moreover, the research team would include top doctors, experts, nurses, health care professionals, data managers, social workers, scientists, and clinical trial coordinators. The participation in the treatments of clinical trials includes both merits and demerits for the participants. So, they need to analyze the trials from different aspects to be able to make the best informed and calculated decisions.
The type of clinical trials known as “treatment” is all about testing new treatments, new approaches to therapy or surgery, and new drug combinations. So, one of the biggest advantages any participant would have is that his diseases might get cured before even the symptoms appear with the help of new treatments rather than the standard ones. It would also open doors to discoveries and new solutions for medical issues or problems. Moreover, the participant would get a chance to serve its humanity and society by saving their lives. Also, there are some genetic diseases as well but the involvement of participants in the treatment of clinical trials would make them have easy access to it for their family members as well.
In addition to the consumption of time, energy, and money of the participants, the treatments of clinical trials also involve some risk factors. The participants must be aware of the risk before giving any consent or signing any agreement with the research team. Any treatment or device can end up causing unintended harm to the participant. So, it is important for the investigator to monitor the treatments and make sure that they are safe and effective. Also, the researchers must follow the strict rules and policies throughout the process of the clinical trial. The careful study plan can also help the researchers if they are ready to follow it properly. Again the investigator would be held responsible to make sure that the plan is being followed without making changes to it.
Now it is clear that treatments of clinical trials have both benefits and risks. However, the risks can be minimized by taking safety precautions and building safeguards into the system. The final decision of participation is solely based on the individual whether they still want to leave a legacy of medical care for their future generations or not. Also, it is advised to consult the clinical trial coordinator to get your queries and confusions addressed beforehand so that you can proceed further with confidence.
