FAQ
What are the symptoms of lupus?
The most common signs may include:1
- Joint pain, stiffness and swelling
- Fatigue
- Fever
- A butterfly-shaped rash on the face that covers the cheeks and bridge of the nose, or rashes that appear elsewhere on the body
- Headaches, confusion and memory loss
- Skin lesions that show up, or worsen, with sun exposure
- Fingers and toes that turn white or blue when exposed to cold or as a result of stress
- Shortness of breath
- Chest pain
- Dry eyes
1. Source: https://www.mayoclinic.org/diseases-conditions/lupus/symptoms-causes/syc-20365789
Who may be a good candidate to apply for a lupus clinical trial?
You should consider applying for a lupus research study if you:
- Are at least 18 years of age or older
- Have had a confirmed diagnosis of any form of lupus
- Are willing and able to attend all appointments (including in-person) at a clinical site for the duration of that study
What are the benefits of participating in a lupus clinical trial?
The information gleaned from clinical studies may help identify new treatment options in the future for people suffering from lupus. Study participants are often connected to specialists who understand their situation and can help answer questions and address concerns. Participants in research studies can expect to enjoy a safe, caring clinical environment, be treated with kindness and respect, and have access to top quality care during the trial.
Are there any costs to participating in a clinical study?
In almost all instances, there is no cost to participate in a clinical trial. Participants receive all study-related medical care and medications for the duration of the study. Likewise in many instances, patients also enjoy benefits such as compensation for time and travel.
Are there any risks to participating?
As all drugs and medical procedures carry a risk of side effects, the possibility that participants may experience some discomfort or other reactions during or after a clinical trial does exist. The study staff for that trial should explain these potential risks before participants decide whether to participate, and help address any concerns.
Does qualifying ensure my participation in a clinical study?
No. The requirements or eligibility criteria vary by clinical trial, and sponsors/clinical sites are constantly looking for various patient populations in order to test the efficacy of their investigational drugs. Further screening will determine whether you’re eligible to participate in an active clinical study, but if not, you will likely be a candidate for one in the future, in which case you may be contacted. At that point, and before a potential participant decides whether to take part in the study, the study staff will review the informed consent form with you and answer any questions. Once the consent form has been signed by the participant (you), the screening period of the study begins.
Can I change my mind about participating in a clinical study?
Participation in clinical trials is entirely voluntary. Even if you are already involved in the study, you can change your mind at any time for any reason.
What if I have more questions?
If you are interested in learning more, please contact us at any time. You may email us at help@clinicalenrollment.com.