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… to gauge their satisfaction with the new system. In addition, information will be collected from participants’ medical records relating to their deliveries and their newborns. … Blood glucose monitoring for pregnant women with diabetes …

… Severe Chronic Neutropenia International Registry … Information from the participant's medical history and medical tests will be released to the Registry office at the University of Washington in Seattle, Washington. The registry … race, referring doctor, diagnosis, medical history, including those of infections, growth and development markers, and records of treatment for neutropenia. The researchers will also ask for information about the health status of the …

… Infants at Risk for Respiratory Distress Syndrome … If you agree to participate, after you sign the consent form, hospital records will be reviewed and reported during the first 7 days of life for your baby. Available health records regarding your pregnancy and delivery will also be reviewed. Health information that will be reported about you will only include information about your pregnancy and delivery such as the types of medication you received, medical conditions you may have had during your pregnancy, and how your baby was delivered. Health information that will be …

… the informed consent, you will be screened to determine if you are eligible to participate. Screening will consist of: medical and obstetric history; collection of demographic information; review of medical records and determination of due date; review of current medications being taken; physical examination; measurement of height …

… will be measured through quality of life questionnaires at baseline, 3 months, 6 months and 12 months as well as their medical records. … Young and strong study …

… biological samples (only blood and tissue is being collected at this time by LVHN) and their associated data (survey data, medical records data, cancer registry data, etc.). People who agree to participate may be asked to fill out medical and health questionnaires as part of their standard medical care visit. Clinical and related data will be collected …

… for 72 hours and will record blood glucose levels every 5 minutes. During this time, patients will continue their usual medical routine, including SMBG and fetal surveillance. After 72 hours the patient will return to the office to have the CGM …

… to clinical trial participation. Clinical information requested by the tool will be obtained from the participant’s medical record by a member of the research team. Patients may be informed about the study, consented and trial data may be …