Texas is currently home to 5071 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Houston, Dallas, San Antonio and Austin. Whether you're a healthy volunteer interested in paid medical research or someone seeking trials related to a specific condition, the state offers a diverse array of opportunities in your vicinity.
Study of Endothelial Cell Condition After Cataract Surgery Performed Using Capsulorhexis or ZEPTO
Recruiting
This study will use images of the subjects' corneal endothelium obtained using non-invasive specular microscopy to obtain corneal endothelial cell density, the coefficient of variation in endothelial cell size, and the percentage of hexagonal endothelial cells following routine cataract surgery performed using the standard method of manual capsulorhexis compared to cataract surgery performed using Zepto Precision Capsulotomy System.
Gender:
All
Ages:
50 years and above
Trial Updated:
03/08/2022
Locations: UltraVision, Eagle Pass, Texas
Conditions: Endothelial Cell Density Loss
Effectiveness of Multichannel Functional Electrical Stimulation
Recruiting
The purpose of this pilot study is to determine whether two weeks of multi-channel FES along with task-specific training will improve UE function when compared to traditional rehabilitation or usual care. The secondary purpose of this study is to find whether two weeks of multi-channel FES along with task-specific training will improve shoulder range of motion, grip strength, and patient reported function when compared to traditional rehabilitation or usual care in patients with unilateral strok... Read More
Gender:
All
Ages:
18 years and above
Trial Updated:
03/08/2022
Locations: Baylor Scott and White Institute for Rehabilitation, Frisco, Texas
Conditions: Stroke, Hemiparesis
Mesenchymal Stromal Cells in Living Donor Kidney Transplantation
Recruiting
Kidney transplantation is a good treatment option for people with kidney disease. However, there is still much to learn about how to best care for the transplanted kidney and keep it functioning for a long time. Transplant recipients receive induction therapy and immunosuppression (anti-rejection) drugs to prevent their body from rejecting the new kidney. These drugs are used to prevent the immune system from attacking the transplanted kidney. This research study will evaluate the safety and act... Read More
Gender:
All
Ages:
Between 18 years and 65 years
Trial Updated:
03/08/2022
Locations: Houston Methodist Hospital System, Houston, Texas
Conditions: Renal Transplantation, Mesenchymal Stem Cells
Prospective Global Registry for the Study of Chronic Total Occlusion Intervention
Recruiting
Percutaneous coronary intervention (PCI) of chronic total occlusions (CTOs) is increasingly being performed in patients with advanced coronary artery disease, but there is limited information on the techniques utilized and the procedural outcomes. The goal of this multicenter, investigator initiated registry is to collect information on treatment strategies and outcomes of consecutive patients undergoing CTO PCI among various participating centers. The information collected will be used to deter... Read More
Gender:
All
Ages:
All
Trial Updated:
03/08/2022
Locations: University of Texas Southwestern Medical Center, Dallas, Texas
Conditions: Coronary Artery Disease
Feasibility of Endovascular Repair of Ascending Aortic Pathologies
Recruiting
The purpose of this early feasibility study is to investigate the outcome of selected patients with ascending thoracic aortic pathologies including type A aortic dissection, who are suitable for endovascular repair with the Medtronic Valiant PS-IDE Stent Graft System with the Captivia Delivery System (or the Valiant PS-IDE Stent Graft).
Gender:
All
Ages:
21 years and above
Trial Updated:
03/07/2022
Locations: Baylor Scott & White The Heart Hospital, Plano, Texas
Conditions: Dissection of Thoracic Aorta
A Study to Evaluate the Safety and Pharmacokinetics of Single and Multiple Doses of Prosetin in Healthy Volunteers
Recruiting
This trial is a Phase 1a/1b, randomized, double-blind, placebo-controlled study designed to assess the safety, tolerability, and pharmacokinetics of single and multiple ascending oral doses of prosetin administered to healthy adult subjects.
Gender:
All
Ages:
Between 18 years and 65 years
Trial Updated:
03/06/2022
Locations: Worldwide Clinical Trials Early Phase Services, San Antonio, Texas
Conditions: Amyotrophic Lateral Sclerosis
KRT-232 and TKI Study in Chronic Myeloid Leukemia
Recruiting
This study evaluates KRT-232, a novel oral small molecule inhibitor of MDM2, for the treatment of patients with Ph+ Chronic Myeloid Leukemia (CML) who have relapsed or are refractory or intolerant to a Tyrosine Kinase Inhibitor (TKI). This study is a global, open label Phase 1b/2 to determine the efficacy and safety of KRT-232 in patients with chronic phase CML (CML-CP) and accelerated phase (CML-AP) who have failed TKI treatments.
Gender:
All
Ages:
18 years and above
Trial Updated:
03/04/2022
Locations: Texas Oncology- Sammons CC at Baylor, Dallas, Texas
Conditions: Chronic Myeloid Leukemia
Reading Remediation and Outcomes in Detention
Recruiting
The current literature on academic skill difficulties, whether considered as part of the continuum of ability or as a specific learning disability (LD), indicates that these problems often coexist with conduct problems and juvenile delinquency, and are risk factors for initial law-breaking behavior and for its persistence. However, less is understood about how this relationship develops. It is these broad questions that this project seeks to address. First, what is the causal pathway? Does LD ca... Read More
Gender:
Male
Ages:
Between 14 years and 16 years
Trial Updated:
02/25/2022
Locations: Burnett-Bayland Rehabilitation Center (BBRC), Houston, Texas
Conditions: Specific Learning Disorder (MeSH Unique ID: D000067559), Dyslexia (MeSH Unique ID: D004410), Conduct Disorder (MeSH Unique ID: D019955)
Comparing 1 Week Versus 2 Week Cutaneous Suture Removal
Recruiting
Our goal is to compare the difference in surgical outcomes and patient satisfaction for surgical scars on the face between suture removal at 1 week versus 2 weeks. There is variation in the timing at which Mohs surgeons remove sutures on the face. Some prefer 1 week, and others prefer 2 weeks. This has not been formally studied. It is possible the outcomes are the same between both groups, or that one has a better cosmetic outcome than the other. Your skin cancer will be removed as usual. Afte... Read More
Gender:
All
Ages:
18 years and above
Trial Updated:
02/24/2022
Locations: DermSurgery Associates, Houston, Texas
Conditions: Suture; Complications, Mechanical, Scar, Surgery
Factorial Trial Testing Guided Thinking Tasks to Optimize a Physical Activity Intervention
Recruiting
The objective of this study is to optimize a novel, audio-recorded physical activity intervention that is scalable. Using principles of the Multiphase Optimization Strategy (MOST) framework, a full factorial study will test the unique and combined effects of different intervention components to identify which combination of components is optimal for increasing physical activity and mechanisms by which the components are or are not effective. This information will inform decisions about an optima... Read More
Gender:
All
Ages:
Between 18 years and 64 years
Trial Updated:
02/24/2022
Locations: Southern Methodist University, Dallas, Texas
Conditions: Physical Inactivity
Evaluation of an Anti-Shivering Protocol Cardiac Arrest
Recruiting
This will be a single center, retrospective, before-and-after, chart review of all patients undergoing TTM between June 1, 2017 and May 31, 2021 at MDMC. Initiation of the new TTM protocol occurred on April 22, 2019.
Gender:
All
Ages:
18 years and above
Trial Updated:
02/21/2022
Locations: Methodist Dallas Medical Center, Dallas, Texas
Conditions: Cardiac Arrest
Brief Prolonged Exposure Therapy Versus Clinical Standard to Reduce Posttraumatic Stress Post Spinal Cord Injury
Recruiting
This study will examine the use brief prolonged exposure (Brief PE) therapy compared to standard clinical care to reduce posttraumatic distress among people who have had a spinal cord injury and are receiving rehabilitation in an inpatient setting.
Gender:
All
Ages:
18 years and above
Trial Updated:
02/15/2022
Locations: Baylor Institute for Rehabilitation, Dallas, Texas
Conditions: Spinal Cord Injuries, PTSD, Post-Traumatic Stress Disorder