Frequently Asked Questions

There are a number of good reasons to consider participating in a clinical trail. In addition to personal attention and individualized care, participants often have access to therapies or FDA-approved medications that may not yet be available to the general public. Trials are also an opportunity to learn more about a medical condition and meet others with similar conditions.

The potential benefits from participating in clinical trials help prove whether a treatment is effective and/or can help determine the safe dosages required and the potential side effects that can occur with a new drug. You also gain the satisfaction of knowing that your participation in the study may lead to advancements that will benefit others in the future.

All medical procedures — even proven therapies — have risks. Every clinical trial is different, but anticipated risks will be reviewed with each potential participant as part of the informed consent process.

Requirements vary depending on the study. Participants will need to meet certain eligibility and screening requirements in advance. If those criteria are met there will be an initial screening examination at which time an informed consent document will be reviewed with the parent/guardian. Once admitted to the program, usually visits to Children's Hospital of Pittsburgh to meet with medical professionals for examination or treatment will be part of the regimen, however the frequency of appointments will vary.

Informed consent is a process that assures you have all the necessary facts about a clinical trial before deciding whether or not to participate. The medical professionals running the study will explain all details and answer all questions. The researchers will provide an informed consent document that provides the study details, purpose, duration, required procedures, risks and potential benefits. The participant then decides whether to sign the document, indicating they reviewed and understood its content. It is not a contract. Participants may withdraw from a trial at any time.

Participants often join clinical trials as a result of a referral from their own pediatricians, but that's not always the case. You will, however, find it helpful to confer with your child's physician and other members of your family or friends about deciding to join a clinical trial.

Patients who participate in clinical studies will not be charged for visits with medical professionals or for equipment, medicines, or materials required by the study.

Cost of research studies are paid in one of two ways. Hospital and laboratory expenses are paid by the grant when such expenses are only for research purposes. Non-research expenses that are part of the treatment of a child's condition will be the patient's financial responsibility and will be charged to the insurance provider. 

Some studies will compensate subjects for time and inconvenience for participation in a trial, but for others, study participants are not paid. Generally expenses associated with visits, such as travel costs or parking while in clinic for study procedures are reimbursed. The study coordinator will explain reimbursements during the informed consent process.

At any given time, Children's has hundreds of studies underway. To see if there is a trial appropriate to you or a member of your family, please search Clinical Trials to view brief descriptions of all current studies.

For further help in guiding your decision, the National Institutes of Health provides a discussion about Clinical Trials, which addresses additional questions you may have.

The identity of participants in a research study is kept confidential. In addition, scientific publications that result from the research do not identify participants without specific prior approval.

All research protocols implemented at UPMC Children’s Hospital of Pittsburgh are carefully examined and reviewed by the Human Research Protection Office (HRPO) of the University of Pittsburgh or the UPMC Office of Sponsored Programs and Research Support (OSPARS). The HRPO and OSPARS offices protect the rights and welfare of individuals recruited to participate in research activities and ensures that only safe, ethical and scientifically valuable research is being considered.