What kind of follow-up is needed if I participate in the Targit Trial?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...Regardless of where you live or which type of radiotherapy you receive, participation in the TargitTrial requires that you meet with the USC doctors every 6 months for the first 5 years, and then annually for an additional 5 years. Each participant is expected to provide her own travel and accommodations for these follow-up visits. Any medical costs associated with these follow-up visits will be billed to your insurance company or to Medicare.
Related QuestionsCan I participate in the Targit Trial if I have already had my breast cancer surgery (lumpectomy)?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...Yes. You may still qualify for the Targit Trial if you have had a lumpectomy within the past 4 weeks for invasive breast cancer. To determine if you are eligible, you will need to be evaluated by a surgeon and radiation oncologist at USC. This evaluation will include physical examination, review of your mammograms and ultrasound, and review of your pathology results.
Related QuestionsCan I participate in the Targit Trial if I need to receive chemotherapy or hormonal therapy?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...Most women with breast cancer are advised to take chemotherapy or endocrine treatment to try to stop the cancer from coming back. Participation in the Targit Trial will not prevent you from receiving these treatments, nor will it interfere with the type, timing, and dosage of these treatments.
Related QuestionsDo I get compensated for participating in the Targit Trial?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...Single-Day Targeted Intraoperative Radiotherapy is currently being evaluated as an alternative to Conventional Postoperative Radiotherapy and may only be obtained by participating in the Targit Trial. Half of the participants in the Targit Trial will receive Single-Day Targeted Intraoperative Radiotherapy at the time of surgery following removal of the breast cancer. The other half will receive Conventional Postoperative Radiotherapy given over a 6-7 week period after recovering from surgery.
Related QuestionsWhen will the results of the Targit Trial be known?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...The results of the Targit Trial may not be analyzed for several years, following strict scientific guidelines as to when this should be done. Until then, the data from the study will be regularly reviewed by a small group of international experts not directly involved in the study (called the Data Monitoring and Safety Committee). They will advise and make recommendations on the safety and conduct of the study.
Related QuestionsWhat are the costs of participating in the Targit Trial?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...After you have been assigned to one of the two treatments, USC will contact your insurance company or Medicare to determine if it will pay for your treatments. If your insurance company or Medicare refuses to pay for your treatments, you may only participate in the Targit Trial if you are willing and able to pay for the treatments yourself. USC will inform you of all associated costs prior to your making a final decision to participate in the Targit Trial.
Related QuestionsWhat are my rights as a participant in the Targit Trial?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...Your participation in the Targit Trial is voluntary. Your decision whether or not to take part will not affect your current or future care at USC. You are not waiving any legal claims or rights. If you do decide to take part in this study, you are free to change your mind and stop being in the study at any time.
Related QuestionsWhat are the possible side effects and risks associated with participating in the Targit Trial?
Intraoperative Radiotherapy for Breast Cancer - Frequently a...Side Effects and Risks Related to Surgery: Side effects and risks related to breast cancer surgery are similar to any cancer removal surgery: infection, bleeding, loss or reduced nerve function, swelling (edema), blood clotting, hematoma (accumulation of blood within the wound), seroma (accumulation of fluid within the wound), wound breakdown, bruising, scarring, and allergic reactions.
Related QuestionsWhat kind of follow-up care is needed?
Change Your SmileGood oral hygiene: Your implants can fail for the same reasons that your natural teeth are lost. Poor oral hygiene is the greatest cause of implant failure. The build-up of dental plaque and debris around teeth and implants cause an increased concentration of bacteria and the destructive consequences of inflammation and infection. This will lead to swollen gums and loss of bone that is needed to support the implant.
Related QuestionsAmerican Institute of Esthetic and Implant DentistryYour implants can fail for the same reasons that your natural teeth are lost. Poor oral hygiene is the greatest cause of implant failure. The build-up of dental plaque and debris around teeth and implants cause an increased concentration of bacteria and the destructive consequences of inflammation and infection. This will lead to swollen gums and loss of bone that is needed to support the implant.Related Questions
Efudex® | FAQ / What to ExpectYou should visit your doctor after therapy to plan your follow-up care, including regular appointments to make sure new lesions are not developing.Related Questions
Can I participate in more than one clinical trial at a time?
Arizona Alzheimer's ConsortiumNo. You can participate in only one intervention study at a time so that the efficacy of the substance being tested will not be confused with the effects of another intervention. It may be possible to volunteer for an observational study and an interventional study simultaneously. For additional information on clinical trials, please visit: http://www.clinicaltrials.gov
Related QuestionsClinical Trial FAQ'sAll clinical trials have guidelines about who can participate. Using inclusion/ exclusion criteria is an important principle of medical research that helps to produce reliable results. The factors that allow someone to participate in a clinical trial are called "inclusion criteria" and those that disallow someone from participating are called "exclusion criteria".Related Questions
What exactly is a clinical trial? Should I participate in one?
Breast Cancer FAQClinical trials are studies that help evaluate a new treatment. Clinical trials attempt to answer scientific questions and to find new and better ways to help cancer patients. An institutional review board (IRB) carefully reviews the study before patients begin participation in the clinical trial. Also, some studies are reviewed by government agencies, such as the National Cancer Institute (NCI) and the National Institutes of Health (NIH).
Related QuestionsWho can participate in the MOMENTUM Clinical Trial?
ORQIS Medical | Frequently Asked QuestionsChronic congestive heart failure patients with acute decompensation who poorly respond to medical therapy may be eligible for participation in the trial.
Related QuestionsCan I participate in another clinical trial after I complete a trial?
Arizona Alzheimer's ConsortiumYes. Typically, most clinical trials will allow a participant into another clinical trial after a period of 30 days upon completion of the previous clinical trial. All research studies are designed to benefit the patient and minimize risk. However, there are certain risks involved with each study. Emergency procedures are taken very seriously. Participants in clinical trials receive careful monitoring by a physician and clinical trials staff.
Related QuestionsNow that my treatment is over, what type of follow-up care is needed?
Frequently Asked Questions About Breast Cancer | Advocate He...Generally, physicians will follow-up with a 6-month visit and exam. Annual exams will probably follow as long as no changes or problems are noted. Follow-up care will vary widely with the type and stage of your cancer, and the surgery and treatment you received following surgery. Your doctor will map out a follow-up program with you, if you ask. Remember that early detection is still the key, so the most important thing you can do is become proficient at performing a self-breast exam.
Related QuestionsWhat kind of follow up care is needed following LASIK?
New York Lasik FAQ'sNew York LASIK surgeon Eric Mandel closely monitors the healing process in order to ensure optimal visual improvement. Unlike some other/older refractive procedures, patients usually do not need to wear a bandage or a contact lens after LASIK. Instead, we recommend that you wear your sunglasses or goggles home from the office and while you sleep that evening. Patients are provided with medicated eye drops for approximately one to two weeks following the procedure.
Related QuestionsWhat kind of room is needed?
HomeWord - Parenting Seminars: FAQAll we need is a room large enough for the parents who attend. Chairs can be set up “theater-style” or you can set up tables and chairs in a classroom style. Church auditoriums, fellowship halls, gymnasiums, youth group rooms, community theaters – anywhere your parents will feel comfortable.
Related QuestionsWhat kind of education is needed?
Diocese of JolietThe full program of preparation for priesthood has been established by the Church in various official documents. Requirements include a theological education, as well as an intensive program of spiritual formation and pastoral preparation. This comprehensive priesthood program is generally four years in length, but Sacred Heart has the capacity to adjust preparation programs according to the background of the applicant.
Related QuestionsDCIS : Frequently Asked QuestionsPatients who take part in clinical trials may have the first chance to benefit from improved treatment methods, and they make an important contribution to medical science. Clinical trials are research studies that involve patients.Related Questions
Rochester Clinical ResearchParticipants in clinical trials can play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.Related Questions
AAMC: Clinical TrialsPlease ask about Clinical Trials that are available to you. By considering Clinical Trials and other treatment choices, you are taking an active role in a decision that affects your life. Anne Arundel Medical Center is an Equal Opportunity Employer and an Equal Opportunity Health Care Provider.Related Questions
Frequently Asked Questions About Research - Norton Healthcar...All clinical trials have guidelines about who can participate. Using inclusion/exclusion criteria is an important principle of medical research that helps to produce reliable results. The factors that allow someone to participate in a clinical trial are called "inclusion criteria" and those that do not allow someone to participate are called "exclusion criteria".Related Questions
Frequently Asked Questions About Clinical Trials – Nov...Participants in clinical trials have an opportunity to play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.Related Questions
Frequently Asked Questions - The Children's Hospital, Colora...Participants in clinical trials gain access to new research treatments before they are widely available. Often the process of collecting information in the study will allow your doctor to find out more about your condition and the effects it has on you. This may allow you to benefit from better treatment after completing the trial. Many patients also derive satisfaction from knowing they are aiding in an effort to help reduce the suffering of other people suffering from the same ailment.Related Questions
