Registration of Clinical Trials - Article Example

Insert Registration of clinical trials Registration of clinical trials is a kind of platform, or it could be a catalog with an intention to register any clinical trials carried out. It however, encourage that all the countries should have clinical trials to help them in the clinical process. The clinical trials register should contain all the information carried out during the clinical trials and contains details about a pediatric, which is older, and it needs to be covered. The trials are carried for ensuring that the information is safety for health purpose like diagnostics and therapy protocols. The correct information obtained through the trials registry is made to the public with the help of transparency tool for the purpose of registration. To add on, clinical registry trials can be accessed more easily since they can be searched according to the diseases, geographical location or even with the drug. The trials, however, are registered by biotech or with the medical company that deals with medications with are sponsored, the organization like contract research organization (CRO). However, it may also be registered with the foundation capable of sponsoring the whole project. Scientist with years have discovered that there is always a probability of publishing positive results from the trials as compared to negative or even the null results where their chances are very rarely but there is an invention of the trials that will address the public of which method the research was used (Meinert). Clinical trials came into existence for use after the outbreak of breast cancer that kills many people that resulted in language authorization as stated in the act of FDA modernization act of 1997. To add on, the stated law requires that only serious or dangerous disease should go through the clinical trials for the purpose of examination for better results (Abbasi). Advantage of clinical trials registration While in the register, the description containing the pediatric clinical trial on how the use of any clinical product in any chemical field is well defined. In addition, it enhances collaborations between the private sector and the community sector by sharing the research from both the parties with the availed data. However, with the clinical register, many of the individuals will be availed of the necessary information that could help them to know about the trials they engage. More so, it helps greatly by reducing any biased information produced since the duplications of wok done are reduced to enhance transparency in any obtained information. These are well enhanced with the specialization of labor since both the parties should know what they are supposed to be done. The clinical trials registration helps in maximum utilizations of research resources since most of the people are trained, and they can handle the case concerning the registration whereabouts throughout the universe. Furthermore, reduce the trials registration helps in contributing more efforts in order to reduce the spread of diseases since most diseases can be eliminated such as breast cancer, and the spread can, however. The system plays an important role if trials can be well managed as well as they can also be managed more easily since there is a record containing all the work performed. However, patients undergoing medications together with the health professionals can have a chance to receive a well comprehensive registry based on their countries. They will also get assurance from the health professions any clinical trials in formations are well reported regarding those with negative or null findings. Since most of the patients will be provided with all the necessary in formations and moves concerning a given steps to be undertaken for the research purpose. The information available as the evidence purpose is made more useful and productive for treatment together with healthcare purpose. In addition, the registry discloses all the trials carried out with an intention of ensuring all the information is availed at the appropriate time required (McGraw). Furthermore, there is a likelihood that most of the clinical trials participants are recruited for any given life and threatening conditions now raising the chances of successful results for the clinical trials. Clinical trial helps most of the patients on the given system are able to receive newer medical treatment that most of the people cannot access since the technique may not be received from the all the world for the benefit of the public. The way the patients are treated is more effective and helpful than the normal treatments reducing the chances of deaths among the people leading to the increase in the number of individuals in the country. The treatment process will be followed step by steps more closely to ensure that effective services are given to the public to control any negligence to be observed by the officials (McFadden). To end on, most of the patients who may be involved in the clinical trials will benefit the breast cancer women by helping them in future time. It also helps in enhancing the ethical rules for the improvement of the research meant for undergoing medical research for the improvement of patients concern towards the medication purpose. There is also the urgency to ensure that any information obtained for the purpose of decision-making in the health sector is well obtained (Consensus Statement on Mandatory Registration of Clinical Trials). Finally, the information can also help in identifying any gap during the clinical trials research Disadvantages of clinical trials registration When undergoing the clinical trials registration, it should be noted that lot of time can be wasted since patients are required to fill in mores forms before the treatment as compared to normal treatment where no forms are required for the registration purpose. It also includes patients with the trial registration have more of the side effects compared to the normal treatment of many of the case cannot be experienced such more easily (Clinical Trials Registration). The new introduced ways of treatment cannot be more effective for handling any client’s diseases since most of the complications during the research process cannot be accurate. After the registration, patients undergoing treatment should carry more tests according to the rules compared to the standard treatment of which few tests may be required. It should also be noted that trials at time are costly and now expensive for the natural purpose to obtain unless with the help of a sponsor can fund the research depending on the number of all the conditions to be covered (Goonaratna). During the trials, the activity may last for years because of the following disease like cancer being the most chronic disease may even take years for the doctors to establish if the cancer treatment could have an effect on the patient. At the trials, some social welfare of an individual can be hindered like sexual activity, the use of alcohols and tobacco with many other drugs for health purposes. In addition, it is difficult to decide on the type treatment since there are complications and confusions of the available treatment ways (HARBAUGH). With the trials registration, it is also evident that most of the patients with given groups may not get newly introduced ways of treatment because some of the may be selected to represents the population. In the EU clinical trials register, some contents like detailed information on for surgical procedures or on the medicals procedure may not be obtained with lack evidence for the authorizations of books coming from the ethics committee. However, it cannot even maintained the investigators site coming from the outside the EU). Moreover, a clinical trial cannot provide all the information on all the medicines invented for the purpose of treatments. Finally, web content in others languages cannot be obtained other than the English language according to the European Union (EU) standards. Works Cited Abbasi, K. Compulsory Registration of Clinical Trials. BMJ 329.7467 (2004): 637-638. Web. Clinical Trials Registration. Arch Gen Psychiatry 63.2 (2006): 128. Web. Clinical Trials Registration Required. Archives of Ophthalmology 124.1 (2006): 94-94. Web. Consensus Statement On Mandatory Registration Of Clinical Trials. Surgery 141.6 (2007): 703-704. Web. Goonaratna, Colvin. Mandatory Registration Of Clinical Trials. Ceylon Med. J. 50.4 (2009): n. pag. Web. HARBAUGH, ROBERT E. Public Registration Of Clinical Trials. Neurosurgery 55.5 (2004): N6. Web. McFadden, Eleanor. Management Of Data In Clinical Trials. New York: Wiley, 1998. Print. McGraw, Michael J. Principles Of Good Clinical Practice. London: Pharmaceutical Press, 2010. Print. Meinert, Curtis L. Clinical Trials. New York: Oxford University Press, 2012. Print. Meinert, Curtis L. Clinical Trials Handbook. Hoboken, N.J.: John Wiley, 2013. Print. Read More