
Search Clinical Trials
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Trial of the Efficacy and Safety of Short and Long Course Radiation Therapy With/Without BMX-001
University of Nebraska
Rectal Cancer
In this Phase 2 study, we will conduct an efficacy and safety study of the combination of
investigational drug BMX-001, with short-course radiotherapy (SCRT) or long-course
chemoradiotherapy (LCCRT) as part of total neoadjuvant therapy in newly diagnosed rectal
adenocarcinoma (RAC) patients. expand
In this Phase 2 study, we will conduct an efficacy and safety study of the combination of investigational drug BMX-001, with short-course radiotherapy (SCRT) or long-course chemoradiotherapy (LCCRT) as part of total neoadjuvant therapy in newly diagnosed rectal adenocarcinoma (RAC) patients. Type: Interventional Start Date: Aug 2022 |
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Evaluating Safety and Feasibility of Transcutaneous Spinal Cord Stimulation Following Traumatic and1
Francis Farhadi
Spinal Cord Stimulation
Electric Stimulation Therapy
Traumatic Spinal Cord Injury
Cervical Myelopathy
The study will be a non-randomized, non-blinded pilot study to analyze the safety and
feasibility of a non-significant risk device, transcutaneous spinal cord stimulation. The
aim is to include 30 total patients, 10 patients in each of 3 groups:
1. Non-traumatic spinal cord injury (ntSCI) with d1 expand
The study will be a non-randomized, non-blinded pilot study to analyze the safety and feasibility of a non-significant risk device, transcutaneous spinal cord stimulation. The aim is to include 30 total patients, 10 patients in each of 3 groups: 1. Non-traumatic spinal cord injury (ntSCI) with diagnosis of degenerative cervical myelopathy and offered surgical intervention. 2. Early tSCI screened during the hospital admission when cervical/thoracic spinal injury was diagnosed. 3. Delayed tSCI (control) screened 6-24 months after acute cervical/thoracic spinal injury. Type: Interventional Start Date: Oct 2024 |
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Prospective Evaluation of Pathways for Preterm Birth
John O'Brien, MD
Preterm Birth
Cervix; Pregnancy
This is a single center, prospective cohort study of pregnant patients at high risk for
spontaneous preterm birth: patient's with history of spontaneous preterm birth, patient's
with a short cervix and patient's symptomatic for preterm birth will be included. A
control cohort of nulliparous patient1 expand
This is a single center, prospective cohort study of pregnant patients at high risk for spontaneous preterm birth: patient's with history of spontaneous preterm birth, patient's with a short cervix and patient's symptomatic for preterm birth will be included. A control cohort of nulliparous patients without a short cervix will be recruited to provide baseline data. Plan to enroll 240 patients identified through our ultrasound unit with goal of 60 patients in each group. Type: Observational Start Date: Feb 2022 |
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Post Approval Study - Evaluate the Long-Term Safety and Effectiveness of the WEB Device
Microvention-Terumo, Inc.
Wide Neck Bifurcation Intracranial Aneurysms
A prospective, multicenter, single arm, interventional study. The target patient
population for this study are adult subjects with WNBAs of the anterior and posterior
intracranial circulation. The primary effectiveness outcome of the study is adequate
intracranial aneurysm occlusion on the 1 year a1 expand
A prospective, multicenter, single arm, interventional study. The target patient population for this study are adult subjects with WNBAs of the anterior and posterior intracranial circulation. The primary effectiveness outcome of the study is adequate intracranial aneurysm occlusion on the 1 year angiogram as adjudicated by a core laboratory. Type: Interventional Start Date: Aug 2022 |
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PT150 Drug for Use in Alcohol Use Disorder
Pop Test Oncology LLC
Alcohol Use Disorder
The goal of this study is to learn if PT150 can reduce the behavioral and physical
effects of stress, alcohol, and alcohol use in people with alcohol use disorder. expand
The goal of this study is to learn if PT150 can reduce the behavioral and physical effects of stress, alcohol, and alcohol use in people with alcohol use disorder. Type: Interventional Start Date: Feb 2025 |
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REmotely Monitored, Mobile Health Supported Multidomain Rehabilitation Program With High Intensity1
Duke University
COVID-19
Critical Illness
ICU Acquired Weakness
PICS
Cardiorespiratory Fitness
Multicenter, prospective, randomized controlled trial providing mobile health supported
physical rehabilitation to 120 patients who have been critically ill with COVID-19 and
who complete at least one exercise session. expand
Multicenter, prospective, randomized controlled trial providing mobile health supported physical rehabilitation to 120 patients who have been critically ill with COVID-19 and who complete at least one exercise session. Type: Interventional Start Date: Feb 2023 |
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Novel Precision Medicine Approach to Treatment of Osteoporosis Based on Bone Turnover
Madhumathi Rao
Age-Related Osteoporosis
Osteoporosis affects 24.5% of women over 65 and results in fracture-related hospital
admissions exceeding those of heart attacks, strokes and breast cancer combined. Current
treatment options do not account for differences between age-related and estrogen
deficiency related osteoporosis, because of1 expand
Osteoporosis affects 24.5% of women over 65 and results in fracture-related hospital admissions exceeding those of heart attacks, strokes and breast cancer combined. Current treatment options do not account for differences between age-related and estrogen deficiency related osteoporosis, because of the need for bone biopsies for determination. This study will establish a paradigm-shifting individualized treatment protocol for age-related osteoporosis and a non-invasive method for its determination, thereby reducing the major health problems and enormous burden on society and the elderly related to this disease. Type: Interventional Start Date: Mar 2022 |
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Autologous suraL nervE Grafting to the Substantia nigrA in Patients With Synuclienopathies
Craig van Horne, MD, PhD
Multiple System Atrophy
Parkinsons Disease
This phase I double-blind study focuses on the safety and feasibility of implanting
autologous peripheral nerve tissue (PNT) into the substantia nigra area of the brain in
persons who have been diagnosed with either Parkinson's disease (PD) or Multiple System
Atrophy (MSA). 7 participants will be e1 expand
This phase I double-blind study focuses on the safety and feasibility of implanting autologous peripheral nerve tissue (PNT) into the substantia nigra area of the brain in persons who have been diagnosed with either Parkinson's disease (PD) or Multiple System Atrophy (MSA). 7 participants will be enrolled, with 4 participants receiving the graft and 3 receiving a sham surgery. Eligible participants will be early in their diagnosis with a lower burden of symptoms. Participants will be followed initially for one year after surgery. Type: Interventional Start Date: Feb 2025 |
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Multisite Inventory of Neonatal-Perinatal Interventions (MINI) Minimum Dataset
The University of Texas Health Science Center, Houston
Infant, Extremely Premature
Obstetric Labor, Premature
Premature Birth
Intensive Care, Neonatal
Intensive Care Units, Neonatal
The goal of the Tiny Baby Collaborative Multicenter Inventory of Neonatal-Perinatal
Interventions (MINI) minimum dataset is to serve as a registry detailing the outcomes and
practices for all deliveries and infants admitted to intensive care at 22-23 weeks'
gestation at participating hospitals. expand
The goal of the Tiny Baby Collaborative Multicenter Inventory of Neonatal-Perinatal Interventions (MINI) minimum dataset is to serve as a registry detailing the outcomes and practices for all deliveries and infants admitted to intensive care at 22-23 weeks' gestation at participating hospitals. Type: Observational [Patient Registry] Start Date: Jan 2019 |