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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Showing 31 - 40 of 331 Clinical Trials
Description:
Patients who use cannabis on a regular basis may be at a greater risk for sedation-related complications. In our dental sedation suite, we routinely sedate patients for oral surgery three days per week. We have recently noted an increase in patients who use cannabis regularly. This study will gather self-reported cannabis use history via a questionnaire, and analyze sedation records to assess cannabis use's effect on sedation. Read More
Eligibility:
-18 or greater years of age and report to our oral surgery clinic for treatment.
-Able to consent to their own medical treatment.
-Willing to sign informed consent and complete the questionnaire.
-Able to comprehend the content of the questionnaire and consent form in English.
Contact(s)
ALLANA LANGEN
alangen@buffalo.edu
+1 716-906-0171
Description:
We are seeking Transradial amputee’s participation in a research study aiming to evaluate a novel controller for a prosthetic wrist. This study investigates the performance of the controller during activities of daily living in a virtual reality environment. Upper limb movement and muscle activation will also be collected using Motion Capture Systems and different types of sensors. Study will be done at Furnas Hall 809, AWEAR Lab, University at Buffalo North Campus. Read More
Eligibility:
- 18 years old or above and have unilateral or bilateral upper limp amputation
- Current and/or New user of any type of prosthetic device
- Non-user of prosthetic devices who have been previously fit but have chosen not to wear it
Contact(s)
Jiyeon Kang
jiyeonk@buffalo.edu
+1 716-645-6063
Description:
Participants with or without multiple sclerosis are needed for this research study on audio-visual cognition. Participants will be asked to complete some short questionnaires and cognitive tasks over the span of approximately 2-3 hours. All testing will be completed in one session at the University at Buffalo's Division of Cognitive and Behavioral Neurosciences Laboratories. Read More
Eligibility:
-Age range 20-65 years
-Normal Hearing and Vision
-DO NOT have the following: severe psychiatric disorder, alcohol or substance abuse or dependence, history of traumatic head injury, neurological disturbances other than multiple sclerosis.
Contact(s)
THOMAS COVEY
tjcovey@buffalo.edu
+1 716-859-7573
Description:
Study to assess the effect of dapagliflozin as compared with placebo in patients with heart failure who have been stabilized during hospitalization for acute heart failure. Patients will be followed for a maximum of 2 months. Read More
Eligibility:
1. Currently hospitalized with AHF with symptoms of AHF.
2. LVEF <40% within the past 12 months
3. Elevated NT-proBNP, >1600 pg/ml
4. > 18 years of age
5. eGFR >30
Contact(s)
KELLEY CAROZZOLO (Bilson)
kjc28@buffalo.edu
+1 716-898-5653
Description:
We invite you to participate in this research study because you've been diagnosed with a spinal condition requiring surgery using pedicle screw instrumentation in your lumbar spine. Your surgeon plans to use the VersaTie tether to prevent breakdown above your spine surgery. The VersaTie tether provides a gradual transition from the unfused to fused spine. The study procedure will take place at Gates Vascular Institute. Read More
Eligibility:
Inclusion Criteria
1. >18 years of age at the time of treatment
2. EOS full body or standing 36” AP & Lateral images of entire spine
3. Posterior spine fusion with pedicle screw fixation construct of 5 or more levels
4. Pedicle screw fixation to be supplemented proximally with NuVasive VersaTie system
5. Upper instrumented vertebra (UIV) terminating at a newly instru...
Contact(s)
Tia Warrick
twarrick@ubns.com
+1 347-482-3733
Description:
The purpose of the study is to see how best to educate people about kidney transplantation and donation. The ECMC kidney patient will get an email invitation to participate. Participant will then fill out a few online surveys and watch several short videos about kidney transplantation / donation for about an hour. Participant will be paid up to $200. Read More
Eligibility:
Adult (18+years)
Advanced kidney failure
English speaking
Contact(s)
LIISE KAYLER
liisekay@buffalo.edu
+1 716-898-5283
Description:
Adult patients with cerebral palsy will be walking on ground and a treadmill. Participants will wear a belt on their waist with sensors connected to a robot. There will be unpleasant sounds generated to provide cues to change walking pattern. Study will take place at UB for six sessions and will take two hours for each session. Read More
Eligibility:
Contact(s)
Jiyeon Kang
jiyeonk@buffalo.edu
+1 716-645-6063
Description:
This study enrolls people who have Mitral Regurgitation (MR) who will be having mitral valve surgery. The purpose of this study is to learn about the effectiveness of the MitraClip™ system for treating patients who are candidates for Mitral Valve (MV) repair surgery. We will compare the MitraClip™ system to MV repair surgery which is the current standard of care for this condition. Read More
Eligibility:
-Adults age 75+ (OR if younger than 75 years, then has other conditions that make them eligible for the study).
-Diagnosed with severe mitral regurgitation.
-Your care team has confirmed that your mitral valve anatomy is suitable for percutaneous repair with the MitraClip device.
Contact(s)
ROBIN STEIN
rmstein3@buffalo.edu
+1 716-888-4859
Description:
This study enrolls people who have suffered a stroke in the past 24 hours. The purpose of this study is to learn if a patient can benefit from a clot removal procedure if they have a stroke scale of 5 or lower. Read More
Eligibility:
-Adults ages 18+
-Diagnosed with acute ischemic stroke and have an objective neurological deficit.
Contact(s)
JENNIFER GAY
jgay@ubns.com
+1 716-888-4811
Description:
This clinical study investigates a new treatment for prostate cancer. ODM-208 (CYP11A1 inhibitor) is the oral study medication that will be taken together with oral glucocorticoid (dexamethasone) and mineralocorticoid (fludrocortisone) replacement therapy. The purpose of this study is to find a safe and effective dose of ODM-208 for the treatment of prostate cancer. The purpose of this study is also to use the results of this study to support development programs of CYP11A1 inhibitors in prostate cancer and other relevant indications. Read More
Eligibility:
1) Males greater than or equal to 18 years. 2) Metastatic disease documented either by a positive bone scan, CT, PET/CT or MRI scan 3) Treatment with at least 1 line of taxane-based chemotherapy in castration-sensitive prostate cancer (CSPC) or in CRPC
Contact(s)
Asif Abidi
ahabidi@buffalo.edu
Showing 31 - 40 of 331 Clinical Trials
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