162 Barnwood Drive, Edgewood, KY 41017   |   Phone: 859-757-1359   |   Cell 859-443-8228   |   FAX 859-331-6600   |   EMAIL
WHY PARTICIPATE IN A CLINICAL RESEARCH
A clinical trial is a research study to determine the efficacy and safety of a new medicine or treatment modality. This is the only way to access new treatment options which may be a safer option than the current option.

  • Most medicine or medical treatment that are widely available now have undergone clinical trials in order to get approval from the FDA.

  • The new medicine or treatment options may be safer and more effective than the current existing medicine or treatment options.

  • Clinical trials are monitored by Institutional Review Board (IRB) which is comprised of a panel of expert physicians, and other professionals to ensure the safety of the patients as well as to ensure that the study is being conducted ethically and as per research protocol.

  • Informed consent is obtained from the participants before they are able to participate in the study. A physician or a research staff responsible for conducting the research will explain to the participant about the side effects, risks, and possible benefits in as much details as possible until the participant is fully satisfied.

  • Privacy of participants is strictly maintained per the HIPAA Laws. Participants remain anonymous at all time.

  • During the trial Otrimed physician, or research staff will stay in touch with the research participant on an ongoing basis to ensure compliance with the research protocol and the safety of the research participant.

  • Call OTRIMED at 859 757 1359 or email at info@otrimed.com to find out if you would qualify for a study at our center.
WHY PARTICIPATE IN A CLINICAL RESEARCH
A clinical trial is a research study to determine the efficacy and safety of a new medicine or treatment modality. This is the only way to accessnew treatment options which may be a safer option than the current option.

  • Most medicine or medical treatment that are widely available now have undergone clinical trials in order to get approval from the FDA.

  • The new medicine or treatment options may be safer and more effective than the current existing medicine or treatment options.

  • Clinical trials are monitored by Institutional Review Board (IRB) which is comprised of a panel of expert physicians, and other professionals to ensure the safety of the patients as well as to ensure that the study is being conducted ethically and per research protocol.

  • Informed consent is obtained from the participants before they are able to participate in the study. A physician or a research staff responsible for conducting the research will explain to the participant about the side effects, risks, and possible benefitsin as many details as possible to the participant's satisfaction.

  • Privacy of participants is strictly maintained per the HIPAA Laws. Participants remain anonymous at all time.

  • During the trial Otrimed physician, or research staff will stay in touch with the research participant on an ongoing basis to ensure the safety of them and compliance with the research protocol.

  • Call OTRIMED at 859 757 1359 or email at info@otrimed.com to find out if you would qualify for a study at our center.
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SEE IF YOU QUALIFY FOR AN INVESTIGATIONAL RESEARCH STUDY!
To speak with an experienced coordinator or nurse regarding our research studies, Please call our office at : 859-757-1359

Our hours are flexible and convenient, and someone will call you back as soon as possible.