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Saint Louis University Mental Status

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181. Study to Assess Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of RO7112689 in Healthy Volunteers and Participants With Paroxysmal Nocturnal Hemoglobinuria

the previous 5 years 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): NCT03157635 Locations Layout table for location information France Institut hematologie Centre Hayem CHU paris Saint-Louis Lariboisiere F Widal Hopital St Louis Paris, France, 75475 Centre (...) by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03157635 Recruitment Status : Active, not recruiting First Posted : May 17, 2017 Last Update Posted : February 28, 2019 Sponsor: Hoffmann-La Roche Information provided by (Responsible Party): Hoffmann-La Roche Study Details Study Description Go to Brief Summary: This is a Phase I/II, first-in-human study consisting of 3 sequential parts and an open-label extension (OLE) in which the safety, tolerability

2016 Clinical Trials

182. Adaptive tDCS for Treatment-Resistant MDD

clinic) 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): NCT02942368 Locations Layout table for location information United States, Missouri Washington University in Saint Louis Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators (...) 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: NCT02942368 Recruitment Status : Active, not recruiting First Posted : October 24, 2016 Last Update Posted : October 18, 2018 Sponsor: Washington University School of Medicine Information provided by (Responsible Party): Washington University School of Medicine Study Details Study

2016 Clinical Trials

183. Postoperative Delirium: Brain Vulnerability and Recovery

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): NCT03110185 Locations Layout table for location information United States, Missouri Barnes-Jewish Hospital/Washington University in St. Louis School of Medicine Saint Louis, Missouri, United States, 63110 Sponsors (...) and Recovery 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: NCT03110185 Recruitment Status : Active, not recruiting First Posted : April 12, 2017 Last Update Posted : January 31, 2019 Sponsor: Washington University School of Medicine Information provided by (Responsible Party): Ben Palanca, Washington

2016 Clinical Trials

184. Evaluating PROMIS(®) Applied Cognition Items In a Sample of Older Adults At Risk for Cognitive Decline (Full text)

by an external rater, and compares PROMIS® Applied Cognition Abilities and Concerns subsets with commonly used "legacy" instruments. PROMIS® correlated with objective legacy measures (the Mini-Mental State Examination [MMSE] and Saint Louis University Mental Status [SLUMS] examination), depression (measured with the Geriatric Depression Scale [GDS]), anxiety, and activities of daily living. PROMIS® and MMSE correlations remained after controlling for depression and anxiety. PROMIS® associated more strongly

2016 Psychiatry research PubMed

185. Detecting Change over Time: A Comparison of the SLUMS Exam and the MMSE in Older Adults At Risk for Cognitive Decline: Stability of the SLUMS Exam versus the MMSE (Full text)

Detecting Change over Time: A Comparison of the SLUMS Exam and the MMSE in Older Adults At Risk for Cognitive Decline: Stability of the SLUMS Exam versus the MMSE To directly compare the 1-year stability of Mini-Mental State Examination (MMSE) score and Saint Louis University Mental Status (SLUMS) examination score and correlate score changes with demographic variables, clinical factors, and functional domains.A sample of 304 study participants was recruited from residential and clinical

2016 CNS neuroscience & therapeutics PubMed

186. A Systematic Evidence Review of the Signs and Symptoms of Dementia and Brief Cognitive Tests Available in VA

without prior diagnosis of dementia. Measures to be compared: Blessed Orientation-Memory-Concentration (BOMC) Test, Mini- Cog, Montreal Cognitive Assessment (MoCA), General Practitioner Assessment of Cognition (GPCOG), St. Louis University Mental Status (SLUMS) Exam, and Short Test of Mental Status (STMS). Outcomes: Likelihood for patients to be appropriately diagnosed and treated for dementia; and adverse consequences of assessment, such as depression and anxiety. Settings: Primary general medicine (...) to the Mini-Mental State Examination (MMSE): Blessed Orientation-Memory- Concentration (BOMC) Test, Mini-Cog, Montreal Cognitive Assessment (MoCA), General Practitioner Assessment of Cognition (GPCOG), St. Louis University Mental Status (SLUMS) Exam, and Short Test of Mental Status (STMS). The MMSE, a widely-used clinical instrument for detecting cognitive impairment, requires payment or permission before it can be reproduced or distributed, under copyright by the Psychological Assessment Resources (PAR

2010 Veterans Affairs Evidence-based Synthesis Program Reports

188. Management of Stroke Rehabilitation

facilities is given primarily at medical centers. Smaller DoD community hospitals may have limited resources to see both inpatients and outpatients relying more on the TRICARE network for on-going stroke rehabilitation services Outcome Measures: The Working Group (WG) agreed on the following health related outcome of post-stroke rehabilitation: • Morbidity (secondary complication) • Mortality • Quality of life • Functional status (physical, cognitive, vocational, social) • Patient satisfaction • Access (...) to care • Utilization of healthcare Version 2.0 VA/DoD Clinical Practice Guideline for the October, 2010 Management of Stroke Rehabilitation Introduction Page - 4 Effective rehabilitation improves functional outcome. An indicator for improvement is the positive change in the Functional Independence Measures (FIM TM ) (UDS MR for1997, 1998) score over a period of time in the post- acute care period. Within the Veterans Health Administration (VHA) this measure is captured in the Functional Status

2010 VA/DoD Clinical Practice Guidelines

189. Thoracic Aortic Disease: Guidelines For the Diagnosis and Management of Patients With

, and errors in diagnosis may account for deaths otherwise attributed to cardiac arrhythmia, myocardial infarction (MI), pulmonary embolism, or mesenteric ischemia. The University HealthSystem Consortium (UHC) is an alliance of more than 100 academic medical centers and af?liate hospitals. UHC’s Clinical DataBase/Resource Man- ager allows comparison of patient-level risk-adjusted out- Table 1. Applying Classi?cation of Recommendations and Level of Evidence *Data available from clinical trials or registries (...) 129 110 157 127 673 6.0 No mention of rupture 1091 1183 1472 1621 1773 7140 63.5 Subtotal 1824 1899 2256 2533 2734 11 246 Aortic (unspeci?ed) 3.0 Dissection 223 310 326 343 339 1541 37.6 Ruptured 9 3 15 9 9 45 1.1 No mention of rupture 310 385 505 612 701 2513 61.3 Subtotal 542 698 846 964 1049 4099 Total No. of cases 20 525 23 098 27 651 31 201 32 797 135 275 Total No. of inpatient discharges 2679334 2777880 3018141 3222542 3297834 14995731 UHC indicates University HealthSystem Consortium. * Note

2010 American College of Cardiology

190. The Patient-Reported Outcomes Project of HCV-TARGET

, United States, 48109 United States, Missouri St Louis University Saint Louis, Missouri, United States, 63104 United States, North Carolina Asheville Gastroenterology Associates Asheville, North Carolina, United States, 28801 University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States, 27599 Wilmington Gastroenterology Associates Wilmington, North Carolina, United States, 28403 United States, Pennsylvania University of Pennsylvania Philadelphia, Pennsylvania, United States (...) (PROP-UP) 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: NCT02601820 Recruitment Status : Completed First Posted : November 10, 2015 Last Update Posted : October 25, 2018 Sponsor: University of North Carolina, Chapel Hill Collaborator: Patient-Centered Outcomes Research Institute Information provided

2015 Clinical Trials

191. Combination Obeticholic Acid (OCA) and Statins for Monitoring of Lipids (CONTROL)

Kansas City Research Institute Kansas City, Missouri, United States, 64131 St. Louis University Saint Louis, Missouri, United States, 63104 United States, North Carolina Duke University Medical Center Durham, North Carolina, United States, 27710 Cumberland Research Associates, LLC Fayetteville, North Carolina, United States, 28304 United States, Ohio Consultants for Clinical Research Cincinnati, Ohio, United States, 45249 United States, Pennsylvania Thomas Jefferson University Philadelphia (...) more. Combination Obeticholic Acid (OCA) and Statins for Monitoring of Lipids (CONTROL) (CONTROL) 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: NCT02633956 Recruitment Status : Completed First Posted : December 17, 2015 Results First Posted : June 4, 2018 Last Update Posted : June 4, 2018 Sponsor

2015 Clinical Trials

192. A Pharmacokinetic and Safety Evaluation of HORIZANT (Gabapentin Enacarbil) in Adolescents With Moderate-to-Severe Primary RLS

by its ClinicalTrials.gov identifier (NCT number): NCT02633657 Locations Layout table for location information United States, California Stanford Sleep Medicine Center Redwood City, California, United States, 94063 United States, Missouri Pacific Research Network Saint Louis, Missouri, United States, 63179 United States, South Carolina SleepMed of South Carolina; SleepMed, Inc. Columbia, South Carolina, United States, 29201 United States, Tennessee Vanderbilt University School of Medicine Nashville (...) the maximum number of saved studies (100). Please remove one or more studies before adding more. A Pharmacokinetic and Safety Evaluation of HORIZANT (Gabapentin Enacarbil) in Adolescents With Moderate-to-Severe Primary RLS (RLS) 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: NCT02633657 Recruitment Status

2015 Clinical Trials

193. An Efficacy and Safety Evaluation of HORIZANT in Adolescents With Moderate-to-Severe Primary RLS

, United States, 46256 Contact: Kristi Mann 317-537-6088 ext 1229 Contact: Kristina Cleveland 317-806-6965 Principal Investigator: Keith Ridel, MD United States, Missouri Pacific Research Network Recruiting Saint Louis, Missouri, United States, 63179 Contact: Dixie Creager 619-294-4302 Contact: Jamie Jjirik Principal Investigator: Stephen Thein, MD United States, New York Dent Neurologic Institute Recruiting Amherst, New York, United States, 14226 Contact: Caroline Kumm 716-558-3492 Contact: A Jamison (...) or more studies before adding more. An Efficacy and Safety Evaluation of HORIZANT in Adolescents With Moderate-to-Severe Primary RLS (RLS) 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: NCT02560766 Recruitment Status

2015 Clinical Trials

194. Comparative Study of Anterior vs. Posterior Surgical Treatment for Lumbar Isthmic Spondylolisthesis

States, 21201 Contact: Steven Ludwig, MD 410-328-8808 Contact: Jael Camacho (410) 328-8808 Principal Investigator: Steven Ludwig, MD Johns Hopkins University Recruiting Baltimore, Maryland, United States, 21287 Contact: Daniel Sciubba, MD 410-955-4424 Contact: Zach Pennington (410) 995-4424 Principal Investigator: Daniel Sciubba, MD United States, Missouri University of Missouri Terminated Columbia, Missouri, United States, 65212 Washington University Recruiting Saint Louis, Missouri, United States (...) Recruitment Status : Recruiting First Posted : October 1, 2015 Last Update Posted : January 15, 2019 See Sponsor: AOSpine North America Research Network Information provided by (Responsible Party): AOSpine North America Research Network Study Details Study Description Go to Brief Summary: The aim of this study is to compare outcomes and cost-effectiveness of anterior versus posterior surgical treatment for lumbar Isthmic Spondylolisthesis. The primary objective is to compare treatment effectiveness

2015 Clinical Trials

195. SUSTAIN-IT: Sustaining Quality of Life of the Aged: Heart Transplant or Mechanical Support?

, 48109 United States, Minnesota University of Minnesota Medical Center-Fairview Health Services Minneapolis, Minnesota, United States, 55454 United States, Missouri Saint Luke's Hospital Kansas City, Missouri, United States, 64111 Washington University Saint Louis, Missouri, United States, 63110 United States, New York Columbia University New York, New York, United States, 10032-3702 United States, Ohio Cleveland Clinic Cleveland, Ohio, United States, 44195 The Ohio State University (OSU) Columbus (...) studies before adding more. SUSTAIN-IT: Sustaining Quality of Life of the Aged: Heart Transplant or Mechanical Support? (SUSTAIN-IT) 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: NCT02568930 Recruitment Status : Active, not recruiting First Posted : October 6, 2015 Last Update Posted : January 25, 2019

2015 Clinical Trials

196. Phase III Trial Assessing the Efficacy and Safety of PXT3003 in CMT1A Patients (PLEO-CMT)

Munster, Germany Principal Investigator: Teresa Sevilla, MD Hospital Universitari i Politécnic La Fe, Valencia, Spain Principal Investigator: Marianne De Visser, MD Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) Principal Investigator: Philip Van Damme, MD UZ Leuven, Belgium Principal Investigator: Mark Roberts, MD Salford Royal NHS Foundation Trust, Manchester, UK Principal Investigator: Florian Thomas, MD Saint-Louis University, Saint-Louis, USA More Information Go to Publications (...) studies before adding more. Phase III Trial Assessing the Efficacy and Safety of PXT3003 in CMT1A Patients (PLEO-CMT) (PLEO-CMT) 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: NCT02579759 Recruitment Status : Completed First Posted : October 20, 2015 Last Update Posted : October 9, 2018 Sponsor: Pharnext

2015 Clinical Trials

197. Study of IPH4102 in Patients With Relapsed/Refractory Cutaneous T-cell Lymphomas (CTCL)

the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02593045 Locations Layout table for location information United States, California Stanford Cancer Center Stanford, California, United States United States, Ohio Ohio State University Columbus, Ohio, United States France Hôpital Saint-Louis Paris, France, 75010 Netherlands Leiden University Medical Center Leiden, Netherlands United Kingdom Guy's Hospital London, United Kingdom (...) , Class III or IV, by New York Heart Association (NYHA) criteria. Patients with any serious underlying medical condition that would impair their ability to receive or tolerate the planned treatment. Patients with dementia or altered mental status that would preclude understanding and rendering of informed consent document. 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

2015 Clinical Trials

198. Connectomics in Psychiatric Classification of Bipolar Disorder and Schizophrenia

States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Christina Pritchard 314-362-6952 Principal Investigator: Daniel Mamah, M.D., MPE Sponsors and Collaborators Washington University Early Recognition Center Investigators Layout table for investigator information Principal Investigator: Daniel Mamah Washington University School of Medicine More Information Go to Layout table for additonal information Responsible Party: Washington (...) more. Connectomics in Psychiatric Classification of Bipolar Disorder and Schizophrenia 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: NCT02756065 Recruitment Status : Recruiting First Posted : April 29, 2016 Last Update

2015 Clinical Trials

199. Natural History of Rett Syndrome & Related Disorders

Sahin, MD, PhD United States, Minnesota Gillette Children's Specialty Healthcare Recruiting Saint Paul, Minnesota, United States, 55101 Contact: Rachel Kotoch, CCRC, BS 651-325-2331 Principal Investigator: Arthir Beisang, MD United States, Missouri Washington University School of Medicine and St. Louis Children's Hospital Recruiting Saint Louis, Missouri, United States, 63110-1093 Contact: Olga Novak 314-454-4267 Principal Investigator: Robin Ryther, MD, PhD United States, New York University (...) 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: NCT02738281 Recruitment Status : Recruiting First Posted : April 14, 2016 Last Update Posted : April 5, 2018 See Sponsor: University of Alabama at Birmingham Collaborators: National

2015 Clinical Trials

200. PREDICTive FactOR of Overall Survival Among Geriatric Assessment Tools and Disease Related Factors in Elderly Patients With High Risk Myelodysplastic Syndromes.

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: NCT02689622 Recruitment Status : Recruiting First Posted : February 24, 2016 Last Update Posted : June 12, 2018 See Sponsor: University Hospital, Toulouse Collaborator: National Cancer Institute, France Information provided by (Responsible Party): University Hospital, Toulouse Study Details Study Description Go to Brief Summary (...) Completion Date : December 2018 Resource links provided by the National Library of Medicine related topics: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: Evaluation of disease prognostic factors Research of disease-related factors, research of comorbidities, geriatric assessment (Mini Mental Status Examination (MMSE), Geriatric Depression Scale-15, Mini Nutritional Assessment, Short Physical Performance Battery, grip strength, Fried criteria, Activities of Daily Living

2015 Clinical Trials

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