Search Clinical Trials
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An Adjunct Test Distinguishing Bacterial From Viral Etiology Improves Resource Utilization and Effi1
The University of Texas Health Science Center, Houston
Respiratory Tract Infections
The purpose of this study is to evaluate overall changes in patient management and
longer-term resource utilization between control and test arms, including (but not
limited to) additional work-up (including other diagnostic tests and consults),
antimicrobial treatments, disposition decisions and h1 expand
The purpose of this study is to evaluate overall changes in patient management and longer-term resource utilization between control and test arms, including (but not limited to) additional work-up (including other diagnostic tests and consults), antimicrobial treatments, disposition decisions and hospital length of stay (LOS) Type: Interventional Start Date: Dec 2023 |
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PARTNER 3 Trial - Aortic Valve-in-Valve
Edwards Lifesciences
Aortic Stenosis
Aortic Stenosis, Severe
This study will assess the safety and effectiveness of the SAPIEN 3/SAPIEN 3 Ultra
transcatheter heart valve (THV) in patients with a failing aortic bioprosthetic valve. expand
This study will assess the safety and effectiveness of the SAPIEN 3/SAPIEN 3 Ultra transcatheter heart valve (THV) in patients with a failing aortic bioprosthetic valve. Type: Interventional Start Date: Jan 2017 |
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Phase 0 Master Protocol for CIVO Intratumoral Microdosing of Anti-Cancer Therapies
Presage Biosciences
Solid Tumor
This is a multi-center, open-label Phase 0 Master Protocol designed to study the
localized pharmacodynamics (PD) of anti-cancer therapies within the tumor
microenvironment (TME) when administered intratumorally in microdose quantities via the
CIVO device in patients with surface accessible solid tu1 expand
This is a multi-center, open-label Phase 0 Master Protocol designed to study the localized pharmacodynamics (PD) of anti-cancer therapies within the tumor microenvironment (TME) when administered intratumorally in microdose quantities via the CIVO device in patients with surface accessible solid tumors for which there is a scheduled surgical intervention. CIVO stands for Comparative In Vivo Oncology. Multiple substudies will include specified investigational agents and combinations to be evaluated. Type: Interventional Start Date: Jul 2021 |
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Cognitive Behavioral Intervention to Reduce Procedural Anxiety Among Woman With High Risk Pregnanci1
University of Colorado, Denver
Procedural Anxiety
High Risk Pregnancy
Fetal Complications
The goals of this study are to determine the feasibility and efficacy of a brief,
single-session cognitive-behavioral intervention for reducing preoperative and
postoperative anxiety and for determining satisfaction with the delivery process in
pregnant women scheduled for Cesarean delivery due to1 expand
The goals of this study are to determine the feasibility and efficacy of a brief, single-session cognitive-behavioral intervention for reducing preoperative and postoperative anxiety and for determining satisfaction with the delivery process in pregnant women scheduled for Cesarean delivery due to complications with their pregnancy. This will be done through a combination of psychoeducation and exposure therapy, where the participants will be walked through the steps of a Cesarean delivery in an operating room that mimics where the patient would actually be delivering. Follow-up will occur during the immediate and extended postpartum periods to determine satisfaction and levels of anxiety. Type: Interventional Start Date: Jul 2020 |
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UTHealth Turner Syndrome Research Registry
The University of Texas Health Science Center, Houston
Turner Syndrome
The investigators will conduct genetic comparisons between Turner Syndrome (TS) patients
with and without Bicuspid Aortic Valve (BAV) to identify causative agents of BAV in
people with TS.
The investigators will correlate the patterns and prevalence of structural heart defects
in TS women with eme1 expand
The investigators will conduct genetic comparisons between Turner Syndrome (TS) patients with and without Bicuspid Aortic Valve (BAV) to identify causative agents of BAV in people with TS. The investigators will correlate the patterns and prevalence of structural heart defects in TS women with emerging molecular data to identify patients who are at high risk for cardiovascular complications Type: Observational [Patient Registry] Start Date: Aug 2015 |
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iGlucose® Remote Patient Monitoring Device as an Adjunct to Routine Glucose Meter Devices for Glyce1
The University of Texas Health Science Center, Houston
Gestational Diabetes
Type2 Diabetes
Pregnancy in Diabetic
The purpose of this study is to investigate whether automation of glucose monitoring data
to facilitate the total number of recommended and completed SMBG checks improve clinical
outcomes for women living with gestational and type 2 diabetes during pregnancy? This is
a RCT expand
The purpose of this study is to investigate whether automation of glucose monitoring data to facilitate the total number of recommended and completed SMBG checks improve clinical outcomes for women living with gestational and type 2 diabetes during pregnancy? This is a RCT Type: Interventional Start Date: Nov 2019 |