The World Health Organization recommends one ultrasound before 24 weeks of pregnancy. Recent developments with technology-assisted ultrasound increase ultrasound access to patients in low- and middle-income countries. This study is the evaluation of the implementation of technology-assisted ultrasounds in 7 antenatal clinics in Zambia. The goal is to understanding the acceptability and feasibility of the ultrasounds, and ultimately to publish information helpful to policymakers and clinic directors involved in implementing similar programs in low-resource settings.
This study is an access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) in pediatric and adult patients with hematologic malignancies and other indications. This protocol will allow access to cord blood units that are unlicensed.
I am providing the first description of a language related to Italian from the south of Italy. This language is in danger of disappearing.
To understand the impact on schools of the new law.
The purpose of the study is to capture the time course of patient-reported improvement with VDZ or UST from baseline to Week 52 (end of study).
The purpose of this study is to gather information about how disruptions in school bus services affect children and families.
Specific Aim 1: Identify standardized and validated quality of life values among patients undergoing surgical management of BPH Specific Aim 2: Identify the prevalence and severity of financial toxicity among patients undergoing surgical management of BPH Specific Aim 3: Characterize subjective patient priorities regarding procedure characteristics and the impact of these on patient clinical decision making.
The primary purpose of this research study is to learn about how the level of a protein called p16 changes in the blood of children, adolescents, and adults with sickle cell disease. This protein can provide information about cellular aging which has not been studied before in patients with sickle cell disease. This can help develop future areas of research into sickle cell disease.
The mission of the Collaborative Islet Transplant Registry (CITR) is to expedite progress and promote safety in islet/beta cell transplantation through the collection, analysis, and communication of comprehensive and current data on all islet/beta cell transplants performed in North America, Europe and Australia.
The main purpose of this study is to determine how much MRTX849 can safely be administered to people. This will include looking at what side effects occur and how often they occur.