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Saint Louis University Mental Status

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121. [Trial of device that is not approved or cleared by the U.S. FDA]

, 20815 United States, Missouri Clayton Sleep Institute Saint Louis, Missouri, United States, 63143 United States, Pennsylvania University of Pennsylvania Philadelphia, Pennsylvania, United States, 19104 Sponsors and Collaborators Philips Respironics Study Documents (Full-Text) Documents provided by Philips Respironics: [PDF] September 18, 2017 More Information Go to Layout table for additonal information Responsible Party: Philips Respironics ClinicalTrials.gov Identifier: Other Study ID Numbers: AI (...) of the Effectiveness and Efficacy of the PowerSleep Device 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: NCT03162328 Recruitment Status : Completed First Posted : May 22, 2017 Results First Posted : January 29, 2019 Last Update Posted : January 29, 2019 Sponsor: Philips Respironics Information provided

2017 Clinical Trials

122. Outcomes of Purpura FULminans in Adults

University Hospital Lilles, France, 59000 Edouard Herriot Hospital Lyon, France, 69003 Melun Hospital Melun, France, 77000 Nice University Hospital Nice, France, 6003 Orléans Hospital Orléans, France, 45000 Saint Louis Hospital Paris, France, 75010 Saint-Antoine Hospital Paris, France, 75012 Pitié-Salpétrière Hospital Paris, France, 75013 Cochin Hospital Paris, France, 75014 Bichat University Hospital Paris, France, 75018 Poissy Hospital Poissy, France, 78300 Poitiers University Hospital Poitiers, France (...) Study (hOPeFUL) 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: NCT03216577 Recruitment Status : Completed First Posted : July 13, 2017 Last Update Posted : March 9, 2018 Sponsor: Henri Mondor University Hospital Collaborator: Fondation de France Information provided by (Responsible Party): Nicolas de

2017 Clinical Trials

123. Communicating Multiple Disease Risks: A Translation of Risk Prediction Science

for location information United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators Washington University School of Medicine Investigators Layout table for investigator information Principal Investigator: Erika Waters, MPH, Ph.D. Washington University School of Medicine More Information Go to Additional Information: Layout table for additonal information Responsible Party: Washington University School of Medicine (...) . Communicating Multiple Disease Risks: A Translation of Risk Prediction Science 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: NCT03255291 Recruitment Status : Completed First Posted : August 21, 2017 Last Update Posted : January 9, 2019 Sponsor: Washington University School of Medicine Information provided

2017 Clinical Trials

124. Brain Health and Development With T1DM

ClinicalTrials.gov identifier (NCT number): NCT03335878 Contacts Layout table for location contacts Contact: Samantha Ranck, MSW 314-362-6514 Contact: Tasha Doty, MA 314-362-7160 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Samantha Ranck, MSW 314-362-6514 Contact: Tasha Doty, MA 314-362-7160 Principal Investigator: Tamara G Hershey, PhD Sponsors and Collaborators Washington (...) 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: NCT03335878 Recruitment Status : Recruiting First Posted : November 8, 2017 Last Update Posted : December 24, 2018 See Sponsor: Washington University School of Medicine Information provided by (Responsible Party

2017 Clinical Trials

125. Shared Medical Decision Making in the Prophylactic Treatment of Bipolar Disorder

, 30029 Contact: Anissa Megzari 04.66.68.42.36 Principal Investigator: Mocrane Abbar APHP - Hôpital Saint Louis-Lariboisière-Fernand-Widal Recruiting Paris, France, 75475 Contact: Frank Bellivier Sponsors and Collaborators Centre Hospitalier Universitaire de Nīmes Investigators Layout table for investigator information Principal Investigator: Ludovic Samalin University Hospital, Clermont-Ferrand More Information Go to Publications automatically indexed to this study by ClinicalTrials.gov Identifier (...) more. Shared Medical Decision Making in the Prophylactic Treatment of Bipolar Disorder (ShareD-BD) 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: NCT03245593 Recruitment Status : Recruiting First Posted : August 10, 2017

2017 Clinical Trials

126. PECS Block vs. Multimodal Analgesia for Prevention of Persistent Postoperative Pain in Breast Surgery

information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Ryan C Guffey, M.D. 314-286-2883 Principal Investigator: Ryan C Guffey, M.D. Sub-Investigator: Mitchell E Fingerman, M.D. Sub-Investigator: Erin Gibbons, M.D. Sub-Investigator: Susan Ironstone, M.D. Sub-Investigator: Arbi Ben Abdallah Sub-Investigator: Rebecca L Aft, M.D. Sub-Investigator: Amy E Cyr, M.D. Sub-Investigator: Julie A Margenthaler, M.D. Sub-Investigator (...) Status : Recruiting First Posted : March 21, 2017 Last Update Posted : January 8, 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: In this double blinded randomized placebo-controlled trial, 160 subjects scheduled for breast surgery involving the axilla will be administered a multimodal pain regimen including acetaminophen, dexamethasone, celecoxib

2017 Clinical Trials

127. MCI: CPAP Treatment of OSA (Memories2)

Recruiting Saint Louis, Missouri, United States, 63130-4862 Contact: Brandye Mazdra 314-566-7038 Principal Investigator: Luqi Chi, MD United States, Pennsylvania University of Pennsylvania Recruiting Philadelphia, Pennsylvania, United States, 19104 Contact: Grace Nathanson 215-746-7465 Principal Investigator: Nalaka Gooneratne, MD United States, Texas University of Texas at Austin Recruiting Austin, Texas, United States, 78701 Contact: Maegen Mackenzie, RN 512-471-9462 Principal Investigator: Kathy (...) 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: NCT03113461 Recruitment Status : Recruiting First Posted : April 13, 2017 Last Update Posted : April 18, 2018 See Sponsor: University of Pennsylvania Collaborator: National Institute on Aging (NIA

2017 Clinical Trials

128. Golimumab in Ulcerative Colitis (UC) Patients With Loss of Response (LOR) Followed by Dose Optimization

: NCT03182166 Recruitment Status : Recruiting First Posted : June 9, 2017 Last Update Posted : November 27, 2018 See Sponsor: Centre Hospitalier Universitaire de Saint Etienne Collaborator: Merck Sharp & Dohme Corp. Information provided by (Responsible Party): Centre Hospitalier Universitaire de Saint Etienne Study Details Study Description Go to Brief Summary: It is planned to enroll 80 UC patients who will require optimization of golimumab after secondary LOR. The review of the study protocol and its (...) approval by an Independent Ethics Committee of the University of Saint Etienne are pending. All patients enrolled will give their written informed consent before being included. This study will be conducted in accordance with the ethical principles that have their origins in the Declaration of Helsinki, in compliance with the approved protocol, good clinical practice and applicable regulatory requirements. Patients will visit the investigator from screening visit to visit 6 at W-1, W0, W2, W4, W8

2017 Clinical Trials

129. Psychosocial Factors of Burn Related Injuries and Perceived Gaps in Service Delivery

Update Posted : May 16, 2018 See Sponsor: St. Louis University Collaborator: Mercy Research Information provided by (Responsible Party): Anne Farina MSW, LCSW, St. Louis University Study Details Study Description Go to Brief Summary: This study will utilize a mixed methods design featuring quantitative assessment of symptoms in conjunction with collecting in-depth qualitative data. In this study, perceived stress, mental health symptoms and behaviors and other variables will be used to test how (...) 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): NCT03094013 Contacts Layout table for location contacts Contact: Anne Farina 314-719-7771 Locations Layout table for location information United States, Missouri Mercy Hospital Recruiting Saint Louis, Missouri, United States, 63141 Contact: Jonathan Pollack, MD 314-251-5570 Sponsors and Collaborators St. Louis University Mercy

2017 Clinical Trials

130. A Study to Evaluate the Safety and Efficacy of TS-121 as an Adjunctive Treatment for Major Depressive Disorder

Brothers Behavioral Health Hospital Hoffman Estates, Illinois, United States, 60169 United States, Massachusetts Boston Clinical Trials Boston, Massachusetts, United States, 02131 United States, Missouri Midwest Research Group - St. Charles Psychiatric Associates Saint Charles, Missouri, United States, 63304 St. Louis Clinical Trials Saint Louis, Missouri, United States, 63141 United States, New Jersey Hassman Research Institute Berlin, New Jersey, United States, 08009 Global Medical Institutes (...) studies (100). Please remove one or more studies before adding more. A Study to Evaluate the Safety and Efficacy of TS-121 as an Adjunctive Treatment for 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. Read our for details. ClinicalTrials.gov Identifier: NCT03093025 Recruitment Status : Terminated (Sponsor decision) First Posted

2017 Clinical Trials

131. The ReNEW Study: Maestro® New Enrollment Post-Approval Study Protocol

Layout table for location information United States, Arizona HonorHealth Recruiting Scottsdale, Arizona, United States, 85258 Contact: Heather Lane 480-323-3000 Principal Investigator: James Swain, MD United States, California Smart Dimensions Weight Loss Recruiting Fountain Valley, California, United States, 92708 Contact: Richard Hoang, PA 714-861-4666 Principal Investigator: Peter C LePort, MD United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United (...) : Maestro® New Enrollment Post-Approval Study Protocol (ReNEW) 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: NCT03145636 Recruitment Status : Recruiting First Posted : May 9, 2017 Last Update Posted : February 15, 2018 See

2017 Clinical Trials

132. Study of AMV564 in Patients With AML

, Illinois Northwestern Recruiting Chicago, Illinois, United States, 60611 Contact: Study Coordinator 312-695-1301 United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 United States, New York Weill Cornell Medical College, The New York Presbyterian Hospital Recruiting New York, New York, United States, 10021 United States, Ohio The Ohio State University Comprehensive Cancer Center Recruiting Columbus, Ohio, United States, 43210 Contact (...) serious underlying medical or psychiatric condition (e.g. alcohol or drug abuse), dementia or altered mental status or any issue that would impair the ability of the patient to understand informed consent or that in the opinion of the investigator would contraindicate the patient's participation in the study or confound the results of the study. Ability to become pregnant. However, female patients who have a negative serum or urine pregnancy test before enrollment and agree to use two highly effective

2017 Clinical Trials

133. Study of TAK-935 as an Adjunctive Therapy in Participants With Developmental and/or Epileptic Encephalopathies

, Kentucky, United States, 40504 United States, Maryland Mid-Atlantic Epilepsy and Sleep Center Bethesda, Maryland, United States, 20817 United States, Missouri The Comprehensive Epilepsy Care Center for Children and Adults Saint Louis, Missouri, United States, 63131 United States, New Jersey Northeast Regional Epilepsy Group Hackensack, New Jersey, United States, 07601 United States, Pennsylvania Thomas Jefferson University Philadelphia, Pennsylvania, United States, 19107 United States, South Carolina (...) studies (100). Please remove one or more studies before adding more. Study of TAK-935 as an Adjunctive Therapy in Participants With Developmental and/or Epileptic Encephalopathies 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: NCT03166215 Recruitment Status : Completed First Posted : May 25, 2017 Last

2017 Clinical Trials

134. Developing and Sustaining Nursing Leadership

Leadership Panel Members Nancy Purdy, RN, PhD Panel Co- Chair Associate Professor Ryerson University Toronto, Ontario Karen Eisler,RN, BScN, MScN, PhD Executive Director Saskatchewan Registered Nurses’ Association Regina, Saskatchewan Pam Pogue, RN, MScN Panel Co-Chair Acting Executive Director Nurse Practitioners’ Association of Ontario Toronto, Ontario Wendy Gifford, RN, PhD Assistant Professor, University of Ottawa Associate Researcher, Saint Elizabeth Ottawa, Ontario Cecile Marville-Williams, RN (...) Mental Health Center Ottawa, Ontario Patricia Donnelly, RN, BSc, BScN, MN Nursing Practice Quality Assurance The Regional Municipality of Halton Public Health Department Oakville, Ontario Vanessa Kee, RN, JD Professional Practice Specialist Ontario Nurses' Association Toronto, Ontario Michelle Freeman, PhD, RN Assistant Professor University of Windsor Windsor, OntarioBEST PRACTICE GUIDELINES WWW.RNAO.ORG BACKGROUND 6 Developing and Sustaining Nursing Leadership * Terms marked with a G this document

2013 Registered Nurses' Association of Ontario

135. Assessment and Management of Foot Ulcers for People with Diabetes, Second Edition

and leadership in advancing the development of BPGs; and Expert Panel Chair Laura Teague, Wound Specialist at Saint Michael’s Hospital in Toronto, Canada, for her exquisite expertise and stewardship of this guideline. Thanks also to RNAO staff Rishma Nazarali, Sarah Xiao, Anastasia Harripaul and Andrea Stubbs, for their intense work in the production of this second edition. Special thanks to the entire BPG Expert Panel for generously providing time and expertise to deliver a rigorous and robust clinical (...) /Search Strategy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 106 Appendix D: University of Texas Foot Classification System – Categories 4-6: Risk Factors for Amputation . . . . . . . 109 Appendix E: University of Texas Foot Classification System – Categories 0-3: Risk Factors for Ulceration . . . . . . . . 110 Appendix F: University of Texas Health Science Center San Antonio Diabetic Wound Classification System . . . . . . 112 Appendix G: PEDIS: Diabetic Foot

2013 Registered Nurses' Association of Ontario

136. Decision Making in Advanced Heart Failure

in an Annual Heart Failure Review Characterization of clinical status Functional ability, symptom burden, mental status, quality of life, and disease trajectory Perceptions from caregiver Solicitation of patient values, goals, and general care preferences Estimation of prognosis Consider incorporating objective modeling data Orient to wide range of uncertainty Review of therapies Indicated heart failure therapies in appropriate patients (BB, ACEI/ARB, AA, CRT, ICD) Treatment of comorbidities (AF, HTN, DM (...) oxygen uptake12 to 14 mL g 1 min 1 5. History of at least 1 hospitalization in the past 6 mo 6. Characteristics should be present despite optimal medical therapy NYHA indicates New York Heart Association. Reprinted from Metra et al, 20 with permission of the publisher. Copyright © 2007, Oxford University Press. Allen et al Decision Making in Advanced Heart Failure 1929 Downloaded from http://ahajournals.org by on March 27, 2019guidance on communication techniques to support these decisions. Its

2012 American Heart Association

137. Suspected Spine Trauma

, Lexington, Kentucky; American Academy of Orthopaedic Surgeons. h Radiology Imaging Associates, Denver, Colorado. i Washington University School of Medicine, Saint Louis, Missouri. j UTHealth- McGovern Medical School, Houston, Texas; neurosurgical consultant. k David Geffen School of Medicine at UCLA, Los Angeles, California. l Medical University of South Carolina, Charleston, South Carolina; North American Spine Society. m University of Utah, Salt Lake City, Utah. n Oregon Health & Science University (...) injury was defined as signs of trauma to the head/neck and if baseline mental status was used to define normal mental status. In light of these findings, performing cervical spine imaging of all blunt trauma patients =65 years of age may be considered, even in patients with lower-risk NEXUS criteria. Under the CCR criteria, all blunt trauma patients >65 years of age should be considered for cervical spine imaging. Radiography Cervical Spine Radiographs have largely been supplanted by CT

2012 American College of Radiology

138. Diagnosis and Treatment of Degenerative Lumbar Spinal Stenosis (Revised 2011)

specialties have participated in the development and re- view of all NASS guidelines. To ensure broad-based representa- tion, NASS has invited and welcomes input from other societies and specialties Evidence Analysis Training of All NASS Guideline Developers NASS has initiated, in conjunction with the University of Al- berta’s Centre for Health Evidence, an online training program geared toward educating guideline developers about evidence analysis and guideline development. All participants in guide (...) 2005;30(8):936-943. 9. Atlas SJ, Tosteson TD, Hanscom B, et al. What is different about worker’s compensation patients? - Socioeconomic predictors of baseline disability status among patients with lumbar radicu- lopathy. Spine. Aug 2007;32(18):2019-2026. 10. Bederman SS, Kreder HJ, Weller I, Finkelstein JA, Ford MH, Y ee AJM. The who, what and when of surgery for the degenera- tive lumbar spine: a population-based study of surgeon factors, surgical procedures, recent trends and reoperation rates. Can

2011 North American Spine Society

139. Hemochromatosis, management

, and Evaluation; H63D, His63Asp mutation; HAMP, hepcidin; HCC, hepatocellular carcinoma; HH, hereditary hemochromatosis; HIC, hepatic iron concentration; HII, hepatic iron index; HJV, hemojuvelin; OLT, orthotopic liver transplantation; PCT, porphyria cutanea tarda; S65C, Ser65Cys mutation; TfR2, transferrin receptor-2; TS, transferrin saturation. From the 1 Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, Saint Louis, MO; 2 Department of Medicine, University of Western (...) F. King, M.D., Endowed Chair in Gastroenterology, Professor of Internal Medicine, Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, Saint Louis University Liver Center, 3635 Vista Avenue at Grand Boulevard, St. Louis, MO 63110-0250. E-mail: baconbr@slu.edu; fax: 314-577-8125. CopyrightV C 2011 by the American Association for the Study of Liver Diseases. View this article online at wileyonlinelibrary.com. DOI 10.1002/hep.24330 Potential con?ict of interest

2011 American Association for the Study of Liver Diseases

140. Detrending Changes the Temporal Dynamics of a Semantic Fluency Task (PubMed)

Detrending Changes the Temporal Dynamics of a Semantic Fluency Task Objective: To study the dynamics of clustering semantic fluency responses and switching between clusters. Methods: We conducted a cross-sectional study of participants (N = 60) in a study of patient reported outcomes who were given the Saint Louis University Mental Status test. Sixty-second animal naming tests were scored for the timing of responses as well as the clustering of responses into semantic categories. Time scores

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2016 Frontiers in aging neuroscience

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