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Saint Louis University Mental Status

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81. Comparison of Therapeutic Strategies With Cholinesterase Inhibitors (SOS TRIAL)

, 06100 Contact: Renaud David 04.92.03.47.70 APHP Hôpital Broca Not yet recruiting Paris, France, 75013 Contact: Olivier HANON 01.44.08.35.03 Hôpital Universitaire de la Pitié Salpêtrière Pavillon François Lhermitte Not yet recruiting Paris, France, 75013 Contact: Stéphane EPELBAUM 01.42.16.75.22 APHP Groupe Hospitalier Saint Louis Lariboisière Fernand Widal CMRR Not yet recruiting Paris, France, 75475 Contact: Claire PAQUET 01.40.05.49.54 CHU La Milétrie Pôle de Gériatrie Not yet recruiting Poitiers (...) . Comparison of Therapeutic Strategies With Cholinesterase Inhibitors (SOS TRIAL) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03454646 Recruitment Status : Not yet recruiting First Posted : March 6, 2018 Last Update Posted

2018 Clinical Trials

82. Periacetabular Osteotomy With and Without Arthroscopic Management of Central Compartment Pathology

doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03481010 Contacts Layout table for location contacts Contact: Geoffrey Wilkin, MD 613-798-5555 ext 10347 Locations Layout table for location information United States, Missouri The Washington University Recruiting Saint Louis, Missouri, United States, 63130 Contact: John C. Clohisy, MD Canada, Ontario Ottawa Hospital (...) one or more studies before adding more. Periacetabular Osteotomy With and Without Arthroscopic Management of Central Compartment Pathology The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03481010 Recruitment Status

2018 Clinical Trials

83. Safety and Efficacy of Pimavanserin in Adults With Parkinson's Disease and Depression

, Missouri Washington University School of medicine Recruiting Saint Louis, Missouri, United States, 63110 United States, New Jersey Bio Behavioral Health Recruiting Toms River, New Jersey, United States, 08755 United States, New York Albany Medical College Recruiting Albany, New York, United States, 12208 David L. Kreitzman, MD, PC Recruiting Commack, New York, United States, 11725 United States, North Carolina Asheville Neurology Specialists, PA Recruiting Asheville, North Carolina, United States (...) adding more. Safety and Efficacy of Pimavanserin in Adults With Parkinson's Disease and Depression The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03482882 Recruitment Status : Recruiting First Posted : March 29, 2018 Last

2018 Clinical Trials

84. EpxCogScreen -- A Phone-based Rapid Cognitive Screen (RCS)

Exclusion Criteria: Patients under the age of 65 Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03569722 Locations Layout table for location information United States, Missouri Saint Louis University Geriatric Clinic Saint Louis, Missouri, United (...) States, 63014 Sponsors and Collaborators Theodore Malmstrom, PhD Investigators Layout table for investigator information Principal Investigator: Theodore K Malmstrom, PhD Saint Louis Univeristy Study Documents (Full-Text) Documents provided by Theodore Malmstrom, PhD, St. Louis University: [PDF] April 10, 2018 More Information Go to Publications: Layout table for additonal information Responsible Party: Theodore Malmstrom, PhD, Primary Investigator, St. Louis University ClinicalTrials.gov Identifier

2018 Clinical Trials

85. Pre-exposure Prophylaxis (PrEP) at Home

States, Missouri Washington University AIDS Clinical Trial Unit Not yet recruiting Saint Louis, Missouri, United States, 63110 Contact: Rupa Patel, MD, MPH 314-454-0058 Sponsors and Collaborators Emory University National Institute of Mental Health (NIMH) Investigators Layout table for investigator information Principal Investigator: Aaron Siegler, PhD Emory University Principal Investigator: Kenneth Mayer, MD Harvard Medical School More Information Go to Layout table for additonal information (...) validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03569813 Recruitment Status : Not yet recruiting First Posted : June 26, 2018 Last Update Posted : December 6, 2018 See Sponsor: Emory University Collaborator: National Institute of Mental Health (NIMH

2018 Clinical Trials

86. Human CNS Tau Kinetics in Tauopathies

: Melissa M Sullivan 314-747-4857 Contact: Melody Li, MS, OTR/L 314-273-6062 Locations Layout table for location information United States, Missouri Washington University in St. Louis School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Melissa M Sullivan 314-747-4857 Contact: Melody Li, MS, OTR/L 314-273-6062 Principal Investigator: Randall J Bateman, MD Sponsors and Collaborators Washington University School of Medicine Association of Frontotemporal Degeneration Tau (...) Consortium Investigators Layout table for investigator information Principal Investigator: Randall Bateman, MD Washington University in Saint Louis Medical School Principal Investigator: Nupur Ghoshal, MD, PhD Washington University in Saint Louis Medical School More Information Go to Layout table for additonal information Responsible Party: Washington University School of Medicine ClinicalTrials.gov Identifier: Other Study ID Numbers: 201703052 First Posted: June 4, 2018 Last Update Posted: August 24

2018 Clinical Trials

87. Treatment of Refractory Systemic Lupus Erythematosus by Allogeneic Mesenchymal Stem Cells Derived From the Umbilical Cord

produced by Nanjing team (Pr Sun) in China. It is also logical to select SLE patients with the same severity criteria as those used worldwide to validate the efficacy of anti-Blys therapies. Similarly, the analysis of the expected results should take into account criteria similar or comparable to those used for the pivotal clinical trials. This trial is a unique opportunity to set up collaboration between Saint-Louis APHP, clinical expert center for cell therapy in AD, and University College London (...) identifier (NCT number): NCT03562065 Contacts Layout table for location contacts Contact: Dominique Farge, MD PhD 142499768 ext +33 Contact: Matthieu RESCHE-RIGON, MD PhD 142499742 ext +33 Locations Layout table for location information France Saint-Louis Hospital Paris, France, 75010 Sponsors and Collaborators Assistance Publique - Hôpitaux de Paris More Information Go to Layout table for additonal information Responsible Party: Assistance Publique - Hôpitaux de Paris ClinicalTrials.gov Identifier

2018 Clinical Trials

88. Study of the Safety and Effectiveness of Motiva Implants®

recruiting Indianapolis, Indiana, United States, 46290 United States, Louisiana The Wall Center for Plastic Surgery Recruiting Shreveport, Louisiana, United States, 71105 United States, Michigan Partners in Plastic Surgery of West Michigan Recruiting Grand Rapids, Michigan, United States, 49546 United States, Missouri Parkcrest Plastic Surgery Recruiting Saint Louis, Missouri, United States, 63141 United States, New Jersey Glicksman Plastic Surgery Recruiting Sea Girt, New Jersey, United States, 08750 (...) of Motiva Implants® The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03579901 Recruitment Status : Recruiting First Posted : July 9, 2018 Last Update Posted : August 15, 2018 See Sponsor: Motiva USA LLC Collaborators: ICON plc

2018 Clinical Trials

89. Does BRV Have Faster Onset Time & Greater Effect Than LEV in Epilepsy Pts Using PPR Pharmacodynamic Efficacy Endpoint

number): NCT03580707 Locations Layout table for location information United States, Missouri The Comprehensive Epilepsy Care Center For Children And Adults Saint Louis, Missouri, United States, 63141 Sponsors and Collaborators Rosenfeld, William E., M.D. Comprehensive Epilepsy Care Center for Children & Adults Utrecht University PRA Health Sciences UCB Biopharma S.P.R.L. Investigators Layout table for investigator information Principal Investigator: William E Rosenfeld, M.D. Comprehensive Epilepsy (...) of saved studies (100). Please remove one or more studies before adding more. Does BRV Have Faster Onset Time & Greater Effect Than LEV in Epilepsy Pts Using PPR Pharmacodynamic Efficacy Endpoint The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03580707 Recruitment Status : Completed First Posted : July

2018 Clinical Trials

90. Creating Physical Objects With 3D Printers to Stimulate Reminiscing for Memory Loss [2 R44 AG049548-02A1]

: Will be administered at Week 0 (prior to first therapy session) to establish a baseline. Measures at Week 8 (midpoint of therapy sessions), and Week 16 (following last therapy session) will determine change from the baseline. ] The primary measure of dementia severity will be the Saint Louis University Mental Status (SLUMS) (Tariq, Tumosa, Chibnall, Perry, 2006). The SLUMS has 11 items, the scores on which are summed together to produce a total score. The maximum possible score is 30. Normal range for high school (...) using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: Child, Adult, Older Adult Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: English speaking Physician diagnosis of early-stage Alzheimer's disease or mild cognitive impairment Score of 10 or above on the brief St. Louis University Mental Status examination (SLUMS). Exclusion Criteria: Contacts and Locations Go to Information from

2018 Clinical Trials

91. North American Prodromal Synucleinopathy Consortium

Washington University Recruiting Saint Louis, Missouri, United States, 63110 Contact: Jennifer McLeland 314-747-6124 Principal Investigator: Yo-El Ju, MD Canada, Quebec McGill University Not yet recruiting Montréal, Quebec, Canada, HGH 2R9 Contact: Amelie Pelletier 514-934-1934 ext 45462 Principal Investigator: Ronald Postuma, MD Sponsors and Collaborators Washington University School of Medicine Mayo Clinic University of Minnesota - Clinical and Translational Science Institute University of California (...) (NAPS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03623672 Recruitment Status : Recruiting First Posted : August 9, 2018 Last Update Posted : August 31, 2018 See Sponsor: Washington University School of Medicine

2018 Clinical Trials

92. Surgery Followed by Risk-Directed Post-Operative Adjuvant Therapy for HPV-Related Oropharynx Squamous Cell Carcinoma: "The Minimalist Trial (MINT)"

research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03621696 Contacts Layout table for location contacts Contact: Douglas Adkins, M.D. 314-747-8475 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Douglas Adkins, M.D. 314-747-8475 Principal Investigator: Douglas Adkins, M.D. Sub (...) studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03621696 Recruitment Status : Recruiting First Posted : August 8, 2018 Last Update Posted : February 7, 2019 See Sponsor: Washington University School of Medicine Information provided by (Responsible Party): Washington University School of Medicine Study Details Study Description Go to Brief Summary: The overarching goal of the MINT trial is to reduce treatment-related toxicity

2018 Clinical Trials

93. Short or Long Interval to Ileostomy Reversal After Ileal Pouch Surgery

Ochsner Clinic New Orleans, Louisiana, United States, 70121 United States, Massachusetts Massuchusetts General Hospital Boston, Massachusetts, United States, 02114 Beth Israel Boston, Massachusetts, United States, 02215 United States, Michigan University of Michigan Ann Arbor, Michigan, United States, 48109 United States, Missouri Washington University Saint Louis, Missouri, United States, 63110 United States, New York New York University New York, New York, United States, 10006 United States, North (...) Interval to Ileostomy Reversal After Ileal Pouch Surgery (SLIRPS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03587519 Recruitment Status : Enrolling by invitation First Posted : July 16, 2018 Last Update Posted : November 29, 2018 Sponsor: University of Colorado, Denver Information provided

2018 Clinical Trials

94. Safety, Tolerability, PK and Efficacy of Single Doses of NV-5138 in Healthy Volunteers and Subjects With Treatment-Resistant Depression

-5757 Principal Investigator: Kerri Louise Wilks, MD Innovative Clinical Research Inc Recruiting Hialeah, Florida, United States, 33012 Contact: Nestor Morillo 786-454-2950 Principal Investigator: Rishi Kakar, MD Research Centers of America Recruiting Hollywood, Florida, United States, 33024 Contact: Peter Ventre, MD 954-990-7649 ext 111 Principal Investigator: Peter Ventre, MD United States, Missouri St. Louis Clinical Trials Recruiting Saint Louis, Missouri, United States, 63141 Contact: Anthony (...) before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03606395 Recruitment Status : Recruiting First Posted : July 30, 2018 Last Update Posted : February 21, 2019 See Sponsor: Navitor Pharmaceuticals, Inc. Information provided by (Responsible Party): Navitor Pharmaceuticals, Inc. Study Details Study Description Go to Brief Summary: Randomized, two-part, placebo-controlled study of single ascending doses of NV-5138 in healthy volunteers, and a single dose of NV-5138 in subjects

2018 Clinical Trials

95. Treatment of Spinal Cord Injury Patients for Neurogenic Bladder: Anticholinergic Agent vs. Mirabegron

edition (WMS-IV) subtest Secondary Outcome Measures : Change in cognitive measure of memory (SLUMS) - baseline and post treatment with mirabegron [ Time Frame: Change from Week 0 to Week 26 ] Saint Louis University Mental Status Exam (SLUMS) - a series of shapes and recall measures Change in cognitive measure of executive function (Stroop test) - baseline and post treatment with mirabegron [ Time Frame: Change from Week 0 to Week 26 ] Stroop Color and Word Test - a series of color-word and picture (...) remove one or more studies before adding more. Treatment of Spinal Cord Injury Patients for Neurogenic Bladder: Anticholinergic Agent vs. Mirabegron (SCIMYR) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03612401 Recruitment Status : Enrolling by invitation First Posted : August 2, 2018 Last Update

2018 Clinical Trials

96. Role of the Gut Microbiome in Complex Regional Pain Syndrome

of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03612193 Contacts Layout table for location contacts Contact: Lara Crock, MD PhD 314-546-3882 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact (...) in Complex Regional Pain Syndrome The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03612193 Recruitment Status : Recruiting First Posted : August 2, 2018 Last Update Posted : January 30, 2019 See Sponsor: Washington University

2018 Clinical Trials

97. Effects of Walking and mHealth Activities for People With Parkinson Disease

Washington University St. Louis Recruiting Saint Louis, Missouri, United States, 63108 Contact: Martha Hessler 314-286-1478 Sponsors and Collaborators Boston University Charles River Campus Washington University School of Medicine Investigators Layout table for investigator information Principal Investigator: Theresa D Ellis, PhD Boston University Principal Investigator: Gammon M Earhart, PhD Washington University School of Medicine More Information Go to Publications: Layout table for additonal (...) disability in PD and perhaps in other chronic progressive conditions. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 220 participants Allocation: Randomized Intervention Model: Parallel Assignment Intervention Model Description: This study will take place at Boston University (BU) and Washington University in St. Louis (WU). This is a two-arm, single-blinded, 1-year randomized controlled trial. Persons with mild to moderate PD

2018 Clinical Trials

98. Combinatorial Pharmacogenomics Testing in Treatment-Naïve Major Depressive Disorder

contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03537547 Contacts Layout table for location contacts Contact: Britt Gott, MS 314-362-2463 Contact: Araba Budu-Anguah, MPH 314-273-1921 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Britt Gott, MS 314-362 (...) adding more. Combinatorial Pharmacogenomics Testing in Treatment-Naïve Major Depressive Disorder The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03537547 Recruitment Status : Recruiting First Posted : May 25, 2018 Last

2018 Clinical Trials

99. Body Scan Activity on Bone Marrow Transplant Patients and Their Caregivers

information United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators Washington University School of Medicine Barnes-Jewish Hospital Investigators Layout table for investigator information Principal Investigator: Maggie Compernolle, BSN, RN Washington University School of Medicine More Information Go to Additional Information: Layout table for additonal information Responsible Party: Washington University School of Medicine (...) Scan Activity on Bone Marrow Transplant Patients and Their Caregivers The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03611764 Recruitment Status : Terminated (Only 5 caregivers decided to participate) First Posted : August 2, 2018 Last Update Posted : October 31, 2018 Sponsor: Washington University

2018 Clinical Trials

100. Short and Long Term Outcomes of Doxycycline Versus Trimethoprim-Sulfamethoxazole for Skin and Soft Tissue Infections Treatment

recruiting Torrance, California, United States, 90509 Contact: Donna Phantran, MPH Principal Investigator: Loren G Miller, MD United States, Missouri Washington University Not yet recruiting Saint Louis, Missouri, United States, 63130 Contact: Mary Boyle Sub-Investigator: Stephanie Fritz, MD Sponsors and Collaborators Los Angeles Biomedical Research Institute National Institute of Allergy and Infectious Diseases (NIAID) Washington University School of Medicine University of California, Los Angeles (...) for details. ClinicalTrials.gov Identifier: NCT03637400 Recruitment Status : Not yet recruiting First Posted : August 20, 2018 Last Update Posted : August 20, 2018 See Sponsor: Los Angeles Biomedical Research Institute Collaborators: National Institute of Allergy and Infectious Diseases (NIAID) Washington University School of Medicine University of California, Los Angeles Information provided by (Responsible Party): loren g miller, Los Angeles Biomedical Research Institute Study Details Study Description

2018 Clinical Trials

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