Trailwire study about hot flushes...
OK someone sent me this knowing I am BC survivor I am not on AI but https://www.geomap-clinicaltrialfinder.com/nct03518138-au-hot-flushes/?fbclid=IwAR1VazAVmQ4InTY8fNBiLKNndKmvBZb6ByZCcbuAfu54l0DpPsgQy1tXyhM https://www.trialwirecontact.com/hot-flashes-au-usa/ I thought some of you might be interested I have put the link here that is the quoted page I have copied below for you as it has the hosptials conducting the trials.. Here are the participating clinics in Australia. Please choose your preferred or nearest.* SYDNEY Women’s Health and Research Institute of Australia SYDNEY Royal North Shore Hospital MELBOURNE School of Public Health and Preventive Medicine MELBOURNE The Royal Womens Hospital PERTH, NedlandS, Sir Charles Gairdner Hospital ADELAIDE Royal Adelaide Hospital HOT FLASHES STUDY (NCT03518138 AU USA) You can register your interest in this breast cancer and hot flashes study here, and get a call back from the Study Coordinator (NCT03518138 AU USA) There was a problem with your submission. Errors have been highlighted below. Firstly, would you like the link for this study information? Yes please send me the link so I can share with friends or my medical specialist Eligibility check - Please check the following applies to you (source ClincalTrials.Gov) Be a female, aged between 18 - 70 years on the day of informed consent Have a history of or current breast cancer and currently taking tamoxifen or an aromatase inhibitor On a stable dose of TAM or an AI for a minimum of 30 days before the Screening Visit and no anticipated need to change the dose for the duration of the study Experience an average of at least 50 moderate to severe hot flashes/week for the 2 weeks immediately preceding the Run-In Visit (i.e., during the Screening period). If on thyroid medication, on a stable dose for a minimum of 30 days before the Screening Visit and no anticipated need to change the dose for the duration of the study If taking an SSRI or SNRI, on a stable dose for a minimum of 30 days before the Screening Visit and no anticipated need to change the dose for the duration of the study Willing and able to complete the daily participant diary, attend all study visits, and participate in all study procedures Able to provide informed consent I have checked the eligibility criteria* Confirmed This field is required. Let's find your nearest participating clinic.* See the participating clinics in the UNITED STATES See the participating clinics in AUSTRALIA Here are the participating clinics in Australia. Please choose your preferred or nearest.* SYDNEY Women’s Health and Research Institute of Australia SYDNEY Royal North Shore Hospital MELBOURNE School of Public Health and Preventive Medicine MELBOURNE The Royal Womens Hospital PERTH, NedlandS, Sir Charles Gairdner Hospital ADELAIDE Royal Adelaide Hospital Please note: These are all HREC registered and approved participating hospitals and clinics. When is the best time to contact you?* Morning? Afternoon? Before or after work? During work hours? Your name* Your name and contact details will ONLY be sent to the clinic team. Your email* (Please always check your junk folder if you don't get an email back from the Study Coordinator) Do you want the clinic contact details also?* Yes please No thanks TECHNICAL SUPPORT If you are having technical problems, please contact us at Team@Trial-Wire.com