There are currently 2867 clinical trials in Houston, Texas looking for participants to engage in research studies. Trials are conducted at various facilities, including M D Anderson Cancer Center, University of Texas MD Anderson Cancer Center, Baylor College of Medicine and The University of Texas - MD Anderson Cancer Center. Whether you're a healthy volunteer looking to participate in paid medical research or seeking trials related to a specific condition, the city provides a diverse range of opportunities near you.
Bacterial Load Reduction by GentleWave and EdgePro Irrigation Systems in Mandibular Necrotic Molars
NCT06554366
Recruiting
The purpose of this study is to compare the efficacy of GentleWave versus EdgePro irrigation in the disinfection of infected root canals of human permanent teeth with necrotic pulp.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
12/04/2024
Locations: The University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Pulp Necroses
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Improving Surgical Patient Outcomes Through Implementation of a SemiStructured Intraoperative Anesthesia Handoff Tool
NCT06533111
Recruiting
The purpose of this study is to assess the impact of a semi-structured intraoperative anesthesia handoff tool on patient outcomes and to assess the validity of the 5-Factor Perceived Shared Mental Model Scale (5-PSMMS) in a healthcare setting and whether the perception of Shared Mental Model (SMM) mediates the effect of the intraoperative handoff tool on postoperative outcomes
Gender:
ALL
Ages:
Between 18 years and 105 years
Trial Updated:
12/04/2024
Locations: The University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Post-operative Complications
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MISC-IPV: a Community-Based Intervention for Children Traumatized by Intimate Partner Violence
NCT05948631
Recruiting
This study adapts and evaluates preliminary outcomes of the Mediational Intervention for Sensitizing Caregivers (MISC) for women and children of color who have survived domestic violence.
Gender:
ALL
Ages:
Between 7 years and 65 years
Trial Updated:
12/04/2024
Locations: University of Houston, Houston, Texas
Conditions: MISC Intervention, Treatment as Usual
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The Will Erwin Headache Research Center - Cluster Headache Study
NCT02910323
Recruiting
The Will Erwin Headache Research Center Study of Cluster Headache and Trigeminal Neuralgia is a prospective, multicenter, observational research network for subjects with Cluster Headache and/or Trigeminal Neuralgia.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
12/04/2024
Locations: The University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Cluster Headache, Cluster Headaches and Other Trigeminal Autonomic Cephalgias, Paroxysmal Hemicrania, SUNCT, Hemicrania Continua, Trigeminal Neuralgia
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A Study to Evaluate ENERGI-F703 GEL in Diabetic Foot Ulcer
NCT05930210
Recruiting
This Phase 3 study is a randomized, double-blind, vehicle-controlled, multiple-center, parallel study to evaluate efficacy and safety of ENERGI-F703 GEL compared with vehicle control in subjects with Wagner Grade 1 to Grade 2 diabetic foot ulcers. Baseline target ulcer size (\<16 cm2 vs ≥16 cm2 ) will be included as a stratification factor. Subjects will be randomized 1:1 to receive ENERGI-F703 GEL or vehicle control using an interactive web response system for randomization to automatically ass... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
12/04/2024
Locations: Mt. Olympus Medical Research, Houston, Texas
Conditions: Diabetic Foot Ulcer, Foot Ulcer, Diabetes Mellitus, Wound
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Meal Delivery and Exercise
NCT04906759
Recruiting
The purpose of this study is to evaluate the effects of a home-based exercise program administered through Meals on wheels (MOW) on gait speed and frailty status and to assess the association between novel serum biomarkers (70 kilodalton heat shock proteins (HSP70),Macrophage Inflammatory Proteins(MIP1b), soluble IL-6 receptor alpha-chain (sIL-6R)) and established but non-specific frailty biomarkers (Interleukin 6 (IL-6), C-reactive protein (CRP), Tumor necrosis factor (TNF-α)) in frail and pref... Read More
Gender:
ALL
Ages:
60 years and above
Trial Updated:
12/04/2024
Locations: The University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Frailty
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intenSive UpPer Extremity Recovery Program for Chronic Stroke (SUPER)
NCT05689502
Recruiting
The purpose of this study is to Investigate the feasibility of a high-quality, high-dose, high-intensity upper extremity therapy program and to assess the treatment effects of a high-quality, high-dose, high-intensity upper extremity therapy program on functional outcomes, motor impairment, and quality of life
Gender:
ALL
Ages:
Between 18 years and 80 years
Trial Updated:
12/04/2024
Locations: The University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Chronic Stroke
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Longitudinal Assessment of Brain Structure and Function in Juvenile-onset Huntington's Disease
NCT05707663
Recruiting
The goal of this observational study is to learn about brain development in Juvenile-onset Huntington's Disease (JoHD). The main questions it aims to answer are: * Is brain development different in JoHD than Adult-onset Huntington's Disease (AoHD)? * Can reliable biomarkers for JoHD be found in brain structure and function? Participants will be asked to complete cognitive tests, behavioral assessments, physical and neurologic evaluation, and MRI. Data collected will be compared to populations... Read More
Gender:
ALL
Ages:
Between 6 years and 30 years
Trial Updated:
12/04/2024
Locations: University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Juvenile Huntington Disease, Juvenile-Onset Huntington Disease
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Enhancing Psychotherapy for Veterans and Service Members with PTSD and Anxiety
NCT05843695
Recruiting
The goal of this clinical trial is to compare two different intensive formats of delivering cognitive-behavioral treatment for people with PTSD and anxiety disorders. The main questions it aims to answer are: * Is iTCBT delivered in individual and group formats more effective than TAU in improving anxiety symptoms and quality of life? * For treatment non-responders, is iTCBT-Enhanced more effective than TAU improving anxiety symptoms and quality of life? * Does iTCBT-Individual produce a larger... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
12/04/2024
Locations: Michael E. DeBakey VA Medical Center, Houston, Texas
Conditions: Posttraumatic Stress Disorder, Anxiety Disorders
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Aerosolized Endotracheal Lidocaine to Avoid Intracranial Pressure Spikes in Patients With Severe Traumatic Brain Injury
NCT05058677
Recruiting
The purpose of this study is to evaluate the effectiveness of nebulized lidocaine before Endotracheal suctioning (ETS) compared to instilled lidocaine and the effectiveness of aerosolized lidocaine versus instilled normal saline before ETS in attenuating the increase of intracranial pressure (ICP) in severe head injured children and to evaluate the feasibility of a trial involving instilled lidocaine and aerosolized lidocaine for the management of ETS and to evaluate the safety of nebulized lido... Read More
Gender:
ALL
Ages:
16 years and below
Trial Updated:
12/04/2024
Locations: The University of Texas Health Science Center at Houston, Houston, Texas
Conditions: Traumatic Brain Injury
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PRIME: PReservIng Memory in Epilepsy
NCT05608408
Recruiting
In this study, participants will receive unilateral Deep Brain Stimulation (DBS) for treatment of epilepsy, with network-based stimulation targets specifically defined using a stereo-electro-encephalographic evaluation and chronic recordings using the Medtronic Percept™ primary cell (PC) Neurostimulator DBS System with BrainSense™ Technology. The hypothesis is that, compared to no stimulation or to standard duty cycle high frequency stimulation, epilepsy neuromodulation using low frequency stimu... Read More
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
12/04/2024
Locations: The University of Texas Science Center at Houston, Houston, Texas
Conditions: Mesial Temporal Lobe Epilepsy
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IV Iron Trial for Anemia Related to Uterine Bleeding in Female Patients Presenting to the Emergency Department
NCT05304442
Recruiting
The primary aim of this randomized trial is to assess the efficacy of IV Ferric Derisomaltose vs Oral Iron in the management of women with severe Iron Deficiency Anemia due to Uterine Bleeding in the emergency department.
Gender:
FEMALE
Ages:
Between 18 years and 65 years
Trial Updated:
12/03/2024
Locations: Ben Taub Hospital, Houston, Texas
Conditions: Anemia, Iron Deficiency, Uterine Bleeding
Register for Updates