Rights and Responsibilities
of Research Participants



1. Know About the Study

You have the right to be informed about the study before you decide whether you wish to participate. Here are some of the things you should know before enrolling:

  • What is the question the research study is hoping to answer?
  • What are the risks and benefits of participating?
  • What are the procedures involved in the research and what will you be expected to do?
  • What should you do if you experience a serious side effect?
  • Will you receive anything for taking part? Will there be costs involved in participating?
  • How long you will be in the study and are there are reasons why it might stop early?
  • Who will have access to your information and what will be done to protect your privacy?

You have the right to a copy of the informed consent form.

2. Not Join or Stop Any Time

Participating in research is completely voluntary. You do not have to participate and you have the right to stop participating even if you have already started.  You have the right to refuse to answer questions you are not comfortable answering.

  • You must talk to the research coordinator about your wish to stop so that she can help you withdraw from the study safely and get information about why you don’t want to be in the study anymore. This is very important information for us because we want to do everything we can to make sure our participants have a good experience.

3. Know Who Is Doing the Research

You have the right to know who is conducting and paying for the research. You should be provided with a phone number for the person in charge of the study (the PI).

4. Know Who You Can Call with Concerns

If you have a question, concern or complaint about your participation in a research study at Penn, you have the right to call the University of Pennsylvania Office of Regulatory Affairs, the group responsible for making sure your rights are respected, at 215-898-2614.




1. Your Decision to Participate

You are responsible for asking questions about the research and taking the time to make a careful decision about whether it is right for you. If you aren’t comfortable or you don’t really have time, you should not enroll.

2. Doing What You Agreed to

You are responsible for faithfully doing what you have agreed to do, for example, using the medicine or device as we ask you to or filling out diaries. This is the point of being in the study.

3. Telling Us About Problems

You are responsible for telling us about how you are doing with the study and if you are experiencing any side effects or other unrelated health issues. Contact your coordinator as soon as possible if you are worried or something affects your ability to participate.

4. Being Honest

You are responsible for giving us honest answers and information.

  • Some of the information we ask for is to protect your safety, to make sure you are not involved in a study that might put you at more risk or experiencing something during a study that is abnormal. Some of the information we ask is to protect the safety of others who will benefit from the results of the research. We need to make sure the people in the study are very similar to the people who we are trying to help with the research. If you don’t end up qualifying for a study because of your answers, it’s not the right study for you but there may be another one in the future that could be.
  • The purpose of the research is to answer a question and you are our partner in finding that answer.  If you don’t give us accurate information, the answer we find is not likely to be completely right. If there is something you don’t feel comfortable telling us, please let us know. We know that some of the questions we ask in women’s health are very personal. We promise to do everything we can to make sure your information stays private.  

5. Telling Us You Want to Withdraw

If you decide you don’t want to participate any more, you are responsible for telling the research coordinator or doctor.

  • Failure to come to appointments or return phone calls or emails will not necessarily withdraw you from a study. We may continue trying to reach you until you tell us you don’t wish to be involved anymore. Please let us know if you wish to end your participation!

6. Showing Up

You are responsible for coming to your appointments on time or calling or emailing in advance to reschedule.


Clinical Trials Now Recruiting!

Active Clinical Trials

Fertility and the BRCA gene

Medical Management of PCOS

Non-hormonal intrauterine device

Research study for women with Heavy Menstrual Bleeding due to Uterine Fibroids


IUD study for current Mirena users

Research Study for Overweight Women with PCOS (Polycystic Ovary Syndrome)