June 27, 2006
The safety of study participants is our top priority. The trial is approved and periodically reviewed by an Institutional Review Board (IRB), which includes doctors, administrators, ethicists, and members of the general public. The safety of clinical trials is reviewed by the U.S. Food and Drug Administration.
Before enrolling in a clinical trial, the investigator will explain the purpose of the trial, its expected benefits, any possible risks or side effects, and what your role will be. This is the time to ask questions! If you want to join the trial, you must sign the informed consent documents. You can leave a clinical trial at any time without penalty.
For further information, see Understanding Clinical Trials.
Principal Investigator
Co-Investigators
Stephen Paget, MD
Mary Crow, MD
Doruk Erkan, MD
Silvia Heidi Norbis
Shaziya Assur
Michelle Perna
Summary
Number of Patients we expect to enroll: 1000. No follow-up visits required. If you or your child decides to participate, we will draw 2 tubes (approximately 3 teaspoons) of blood from a vein in your arm. We will also ask you or your child some general questions along with some information about your/his/her medical history. The blood you or your child donates will be stored in a registry and used by scientists at HSS and other institutions for research studies on Systemic Lupus Erythematosus and/or Anti-Phospholipid Syndrome. All information identifying you or your child as a participant in this study will be kept confidential. All records and blood samples will be coded and stripped of all personal identifiers to ensure confidentiality. Your participation in this study should take approximately 15 minutes.
Inclusion/Exclusion Criteria
In order to be eligible for the Autoimmune Disease Registry and Repository, you must have an unequivocal diagnosis of SLE and/or Anti-Phospholipid Syndrome; be over the age of 14 years; and not be pregnant.
Contact Information
Michelle Perna
Clinical Research Coordinator
pernam@hss.edu
212.774.2223