Search and volunteer to participate in these available studies at UB. Your participation in research doesn't just benefit you, it helps advance healthcare for our entire community.
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Description:
This study enrolls children with diagnosed with diabetic ketoacidosis (DKA) who will be admitted to the pediatric intensive care unit (PICU) for treatment. The purpose of this study is to compare the length of time patients have high acid in their blood and how long they have to stay in the hospital with DKA when they are treated with different types of IV fluids in the PICU. Read More
Eligibility:
Children ages 0-18 years old.
Children who present with diabetic ketoacidosis and require pediatric intensive care unit admission.
Children who present with diabetic ketoacidosis and require pediatric intensive care unit admission.
Contact(s)
Description:
We are looking for healthy volunteers ages 18-39 for a study on body composition, standing, and reclining. Read More
Eligibility:
This study is not currently recruiting from this website
Description:
The purpose of this study is to develop a new treatment for tuberculosis (TB). It is expected that direct participation in this study will be during participants' blood draw. Read More
Eligibility:
Healthy Adult
Ages 18-65
Willing to serve as a control in the study
Ages 18-65
Willing to serve as a control in the study
Contact(s)
Description:
This study enrolls people who have recently undergone a Transcatheter Aortic Valve Replacement (TAVR) procedure at Gates Vascular Institute. The purpose of the study is to learn more about the pros and cons of the TAVR procedure. Read More
Eligibility:
Adults ages 18+.
People presenting to the TAVR clinic for an initial visit, a 1 month follow up visit or a 1 year follow up visit.
People presenting to the TAVR clinic for an initial visit, a 1 month follow up visit or a 1 year follow up visit.
Description:
The Buffalo Research Registry connects people 18 years of age and older in Western New York to research opportunities at the University at Buffalo. Read More
Eligibility:
Age 18+
Contact(s)
Description:
This is a research study which will determine whether a series of tests can predict the Read More
Eligibility:
• Coronary artery disease (by cardiac catheterization or definite myocardial infarction)
• ICD implantation for the primary prevention of SCA
• Optimal medical therapy for heart failure [angiotensin converting enzyme inhibitor (ACEI) or angiotensin receptor antagonist (ARA)].
• ICD implantation for the primary prevention of SCA
• Optimal medical therapy for heart failure [angiotensin converting enzyme inhibitor (ACEI) or angiotensin receptor antagonist (ARA)].
Contact(s)
Description:
We are looking for healthy adults age 21+ for a research study. The purpose of this study is to learn more about how bacteria in the mouth work. We hope that with this understanding, new treatments can be designed to prevent disease. Read More
Eligibility:
Age 21+.
In general good health.
Pregnant women may not participate.
In general good health.
Pregnant women may not participate.
Contact(s)
Description:
The purpose of this study is to create a data registry of anterior cruciate ligament (ACL) reconstructions performed at UBMD Orthopaedics & Sports Medicine. Read More
Eligibility:
Patients undergoing ACL reconstruction by one of the study investigators at UBMD Orthopaedics & Sports Medicine
English speakers
English speakers
Contact(s)
Description:
This study enrolls babies with neonatal opioid withdrawal syndrome (NOWS). The purpose of this study is to learn about how babies with this syndrome grow and develop. This will help us learn the best way to care for babies with NOWS. Read More
Eligibility:
Infants born at 36 weeks gestation or greater
Managed for NOWS at Oishei Children's Hospital
Managed for NOWS at Oishei Children's Hospital
Contact(s)
Description:
This study enrolls people who have been diagnosed with Tricuspid Regurgitation (TR) and have Heart Failure symptoms which are not under control despite treatment with current available therapies. The purpose of this study is to compare a new investigational (experimental) device plus optimal drug therapy with optimal drug therapy alone. Read More
Eligibility:
Adults ages 18+
Diagnosed with moderate or greater Tricuspid Regurgitation/Insufficiency with Heart Failure symptoms
Diagnosed with moderate or greater Tricuspid Regurgitation/Insufficiency with Heart Failure symptoms
Contact(s)
Not finding what you are looking for? Add your profile to the
Buffalo Research Registry or
ResearchMatch to be matched with future studies.
