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Saint Louis University Mental Status

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101. Resistance Exercise and Low-Intensity Physical Activity Breaks in Sedentary Time to Improve Muscle and Cardiometabolic Health

vigorous intensity PA Saint Louis University Mental State (SLUMS) score < 21 Evidence or self-report history of deep vein thrombosis, pulmonary embolism, cardiovascular, peripheral vascular, cerebral vascular, pulmonary, or renal disease Evidence or self-report history of type 1 or 2 diabetes mellitus Evidence or self-report history of a bleeding disorder Evidence or self-report history of recurrent vasovagal episodes Evidence or self-report history of severe depression, Schizophrenia, bipolar disease (...) . Read our for details. ClinicalTrials.gov Identifier: NCT03771417 Recruitment Status : Recruiting First Posted : December 11, 2018 Last Update Posted : February 27, 2019 See Sponsor: Louisiana State University and A&M College Collaborators: Pennington Biomedical Research Center National Institute on Aging (NIA) Information provided by (Responsible Party): Brian Irving, Louisiana State University and A&M College Study Details Study Description Go to Brief Summary: What are the effects of resistance

2018 Clinical Trials

102. Feasibility and Efficacy Study of Student Wellness Online Course for Medical Students

staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03039660 Locations Layout table for location information United States, California Stanford University Stanford, California, United States, 94305 United States, Missouri Washington University in St Louis Saint Louis, Missouri, United States, 63130 United States, New Jersey Rutgers Robert Wood Johnson Piscataway, New Jersey, United States, 08854 Sponsors (...) adding more. Feasibility and Efficacy Study of Student Wellness Online Course for Medical Students 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: NCT03039660 Recruitment Status : Active, not recruiting First Posted : February 1, 2017 Last Update Posted : October 4, 2017 Sponsor: Stanford University

2017 Clinical Trials

103. Innovative Minimally Invasive Options in Treatment of Urinary Problems Related to Prostate Enlargement (BPH) in Men

irradiation or radical pelvic surgery Allergy to iodinated contrast agents 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): NCT03043222 Locations Layout table for location information United States, Missouri Saint Louis University Saint Louis, Missouri (...) , United States, 63110 Sponsors and Collaborators St. Louis University Investigators Layout table for investigator information Principal Investigator: Keith Pereira, MD Saint Louis University Hospital Principal Investigator: Beneranda Sophia Ford-Glanton, MD Saint Louis University Hospital More Information Go to Publications of Results: Layout table for additonal information Responsible Party: Keith Pereira, MD:, MD, Assistant professor, Interventional Radiology, St. Louis University ClinicalTrials.gov

2017 Clinical Trials

104. Self-Management App for Patients With Left-Ventricular Assist Devices

using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03049748 Contacts Layout table for location contacts Contact: Jesus Casida, PhD 313-204-7665 Contact: Debra Barton, PhD (734) 763-3868 Locations Layout table for location information United States, Missouri Barnes-Jewish Hospital/Washington University Recruiting Saint Louis, Missouri, United States, 63108 Contact: Heidi Craddock, MSN 314-651-9356 Contact: Danyelle (...) App for Patients With Left-Ventricular Assist Devices 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: NCT03049748 Recruitment Status : Recruiting First Posted : February 10, 2017 Last Update Posted : March 15, 2018 See

2017 Clinical Trials

105. ADDIA Proof-of-Performance Clinical Study

University Hospital, Strasbourg Centre Hospitalier Universitaire Vaudois IRCCS Centro San Giovanni di Dio Fatebenefratelli Hôpitaux Civils de Colmar Istanbul University Assistance Publique - Hôpitaux de Paris University Hospital, Lille University Hospital, Geneva Cliniques universitaires Saint-Luc- Université Catholique de Louvain Erasme University Hospital University Hospital, Montpellier Centre Hospitalier Universitaire de Besancon Centre Hospitalier Universitaire de Nice Information provided (...) universitaires Saint-Luc- Université Catholique de Louvain Erasme University Hospital University Hospital, Montpellier Centre Hospitalier Universitaire de Besancon Centre Hospitalier Universitaire de Nice Investigators Layout table for investigator information Principal Investigator: Frédéric Blanc, MD Hôpitaux Universitaires Strasbourg Principal Investigator: Jean-François Démonet, MD Centre Hospitalier Universitaire Vaudois, Lausanne Principal Investigator: Hakan Gurvit, MD Istanbul University, Istanbul

2017 Clinical Trials

106. Single-Ascending-Dose Study of BIIB076 in Healthy Volunteers and Participants With Alzheimer's Disease

, Missouri St Louis Clinical Trial Recruiting Saint Louis, Missouri, United States, 63141 United States, Texas Covance Dallas CRU Active, not recruiting Dallas, Texas, United States, 75247 United States, Wisconsin Covance CRU Active, not recruiting Madison, Wisconsin, United States, 53704 Sponsors and Collaborators Biogen Investigators Layout table for investigator information Study Director: Medical Director Biogen More Information Go to Layout table for additonal information Responsible Party: Biogen (...) Status : Recruiting First Posted : February 17, 2017 Last Update Posted : January 10, 2019 See Sponsor: Biogen Information provided by (Responsible Party): Biogen Study Details Study Description Go to Brief Summary: The primary objective of the study is to evaluate the safety and tolerability of single-ascending intravenous (IV) infusions of BIIB076 in healthy volunteers and participants with Alzheimer's disease (AD). A secondary objective of the study for both healthy volunteers and participants

2017 Clinical Trials

107. A Study to Assess the Anti-fatigability Effect of CK-2127107 in Elderly Male and Female Subjects With Limitations in Mobility

information United States, Florida University of Florida Gainesville, Florida, United States, 32611 United States, Massachusetts Tufts Medical Center Boston, Massachusetts, United States, 02111-1524 United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110-1010 United States, North Carolina Wake Forest University School of Medicine Winston-Salem, North Carolina, United States, 27157 United States, Ohio Ohio University Heritage College Athens, Ohio, United (...) the maximum number of saved studies (100). Please remove one or more studies before adding more. A Study to Assess the Anti-fatigability Effect of CK-2127107 in Elderly Male and Female Subjects With Limitations in Mobility 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: NCT03065959 Recruitment Status

2017 Clinical Trials

108. DNS-7801 vs. Placebo in Parkinson's Disease

States, 33486 University of South Florida Parkinson's Disease and Movement Disorders Center Tampa, Florida, United States, 33613 United States, Michigan Quest Research Institute Farmington, Michigan, United States, 48334 United States, Missouri Washington University Saint Louis, Missouri, United States, 63110 United States, North Carolina The Neurological Institute PA Charlotte, North Carolina, United States, 28204 United States, Washington Premier Clinical Research Spokane, Washington, United States (...) 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: NCT03306329 Recruitment Status : Terminated (Administrative) First Posted : October 11, 2017 Last Update Posted : February 1, 2018 Sponsor: Dart NeuroScience, LLC Information provided by (Responsible Party): Dart NeuroScience, LLC Study Details Study Description Go to Brief

2017 Clinical Trials

109. Supporting and Enhancing NICU Sensory Experiences (SENSE)

Experiences (SENSE) (SENSE) 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: NCT03316547 Recruitment Status : Active, not recruiting First Posted : October 20, 2017 Last Update Posted : January 23, 2019 Sponsor: Washington University School of Medicine Information provided by (Responsible Party): Roberta (...) Pineda, Washington University School of Medicine Study Details Study Description Go to Brief Summary: Seventy preterm infants born less than or equal to 32 weeks gestation will be put into either the sensory-based intervention (experiment) group or traditional care (control) group. Consecutive admissions at St. Louis Children's Hospital (SLCH) who are hospitalized in a private NICU room will be recruited. The parents of infants in the sensory-based intervention group will be educated and supported

2017 Clinical Trials

110. Text Based Mobile Technology and Weight Loss

University in St. Louis Saint Louis, Missouri, United States, 63105 Sponsors and Collaborators Washington University School of Medicine Investigators Layout table for investigator information Principal Investigator: Diana Parra Washington University School of Medicine More Information Go to Layout table for additonal information Responsible Party: Washington University School of Medicine ClinicalTrials.gov Identifier: Other Study ID Numbers: 201704048 First Posted: June 29, 2017 Last Update Posted (...) 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: NCT03203655 Recruitment Status : Completed First Posted : June 29, 2017 Last Update Posted : February 15, 2019 Sponsor: Washington University School of Medicine Information provided by (Responsible Party): Washington University School of Medicine Study Details Study

2017 Clinical Trials

111. Helping Poor Smokers Quit

): NCT03194958 Contacts Layout table for location contacts Contact: Christina D Roberts, MPH 314-935-2721 Locations Layout table for location information United States, Missouri Washington University in St. Louis Recruiting Saint Louis, Missouri, United States, 63130 Contact: Matthew Kreuter, PhD 314-935-3701 Contact: Amy McQueen, PhD 314-935-3715 Sponsors and Collaborators Washington University School of Medicine National Institutes of Health (NIH) National Cancer Institute (NCI) Investigators Layout table (...) 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: NCT03194958 Recruitment Status : Recruiting First Posted : June 21, 2017 Last Update Posted : July 26, 2018 See Sponsor: Washington University School of Medicine Collaborators: National Institutes of Health (NIH) National Cancer Institute (NCI

2017 Clinical Trials

112. Remediation of Age-related Cognitive Decline: Vortioxetine and Cognitive Training

of Medicine Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators Washington University School of Medicine Queen's University Takeda Investigators Layout table for investigator information Principal Investigator: Eric Lenze, MD Washington University School of Medicine More Information Go to Publications: Layout table for additonal information Responsible Party: Washington University School of Medicine ClinicalTrials.gov Identifier: Other Study ID Numbers: 201509107 First Posted: September (...) more. Remediation of Age-related Cognitive Decline: Vortioxetine and Cognitive Training (BBS) 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: NCT03272711 Recruitment Status : Active, not recruiting First Posted : September 5, 2017 Last Update Posted : January 24, 2019 Sponsor: Washington University

2017 Clinical Trials

113. Hearing Loss in Older Adults Study

Not yet recruiting Los Angeles, California, United States, 90057 Contact: Eric Wilkinson, MD 213-483-9930 Contact: John Galvin, PhD 310-666-7573 United States, Missouri Washington University Not yet recruiting Saint Louis, Missouri, United States, 63112 Contact: Jill Firszt, PhD Contact: Laura Holden, AuD United States, New York New York Eye and Ear Infirmary of Mount Sinai Not yet recruiting New York, New York, United States, 10029 Contact: Maura Cosetti, MD Contact: Samantha Udondem 212-241-3942 (...) 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: NCT03382769 Recruitment Status : Not yet recruiting First Posted : December 26, 2017 Last Update Posted : March 25, 2019 See Sponsor: Cochlear Collaborators: CogState Ltd. Syneos Health Information provided by (Responsible Party): Cochlear

2017 Clinical Trials

114. Suicide Prevention Algorithm in the French Overseas Territories

de Pointe à Pitre Not yet recruiting Les Abymes, Guadeloupe, 97189 Contact: Jean-Michel GAL, MD +590590891123 CH de Monteran Not yet recruiting Saint-claude, Guadeloupe, 97120 Contact: Geoffrey MARCAGGI, MD +590590805252 Martinique CHU Martinique Recruiting Fort-de-France, Martinique, 97261 Contact: Corine CARPIN, Master 1 (0)596592696 ext +596 Principal Investigator: JEHEL Louis, MD, PhD Réunion Etablissement Psychiatrique de Santé Mentale Recruiting Saint-Benoit, Réunion, 97470 Contact (...) in the French Overseas Territories (APSOM) 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: NCT03427190 Recruitment Status : Recruiting First Posted : February 9, 2018 Last Update Posted : October 25, 2018 See Sponsor: University

2017 Clinical Trials

115. Postoperative Delirium: EEG Markers of Sleep and Wakefulness

/Washington University in St. Louis School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Principal Investigator: Ben Palanca, MD, PhD, MSc Sponsors and Collaborators Washington University School of Medicine Investigators Layout table for investigator information Principal Investigator: Ben Palanca, MD, PhD Washington University in St Louis SOM More Information Go to Layout table for additonal information Responsible Party: Washington University School of Medicine ClinicalTrials.gov (...) of Sleep and Wakefulness 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: NCT03291626 Recruitment Status : Recruiting First Posted : September 25, 2017 Last Update Posted : October 30, 2018 See Sponsor: Washington University

2017 Clinical Trials

116. Adaptive Design Study of NEST sTMS in Subjects With Major Depressive Disorder

, Minnesota Mayo Clinic Rochester, Minnesota, United States, 55905 United States, Missouri Washington University/Barnes Jewish Hospital Saint Louis, Missouri, United States, 63110 United States, New York New York University New York, New York, United States, 10016 United States, Oklahoma Laureate Institute for Brain Research Tulsa, Oklahoma, United States, 74136 United States, Pennsylvania University of Pennsylvania Philadelphia, Pennsylvania, United States, 19104 United States, Rhode Island Butler (...) . Adaptive Design Study of NEST sTMS in Subjects With 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: NCT03288714 Recruitment Status : Active, not recruiting First Posted : September 20, 2017 Last Update Posted : January 16, 2019 Sponsor: NeoSync, Inc. Information provided

2017 Clinical Trials

117. Effects of Bright Light on Co-occurring Cancer-related Symptoms in Breast Cancer Survivors

. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03304587 Contacts Layout table for location contacts Contact: Horng-Shiuann Wu, Ph.D., RN 314-454-8929 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Horng-Shiuann Wu, Ph.D., RN 314-454-8929 Principal Investigator: Horng-Shiuann Wu, Ph.D., RN Sub-Investigator: Jean E Davis, Ph.D., RN, FAAN Sub (...) studies before adding more. Effects of Bright Light on Co-occurring Cancer-related Symptoms in Breast Cancer Survivors 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: NCT03304587 Recruitment Status : Recruiting First Posted

2017 Clinical Trials

118. Robotic-assisted and Laparoscopic Right Colectomy Study

States, 48197 Contact: Elizabeth Goetz 734-712-8252 Principal Investigator: Robert Cleary, MD Sub-Investigator: Amanda McClure, MD United States, Minnesota University of Minnesota Recruiting Minneapolis, Minnesota, United States, 55455 Contact: Sara Eischen 612-626-2498 Principal Investigator: Wolfgang B Gaertner, MD United States, Missouri Washington University at St. Louis Recruiting Saint Louis, Missouri, United States, 63110 Contact: Michelle Sperry 314-362-2646 Principal Investigator: Matthew (...) . Robotic-assisted and Laparoscopic Right Colectomy Study - Intracorporeal vs. Extracorporeal Anastomoses (ANCOR) 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: NCT03312569 Recruitment Status : Recruiting First Posted : October

2017 Clinical Trials

119. What Matters Most: Choosing the Right Breast Cancer Surgery for You

ClinicalTrials.gov identifier (NCT number): NCT03136367 Locations Layout table for location information United States, Missouri Washington University in St. Louis Saint Louis, Missouri, United States, 63110 United States, New Hampshire Norris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center Lebanon, New Hampshire, United States, 03756 United States, New York Montefiore Medical Center Bronx, New York, United States, 10467 Bellevue Hospital Center New York, New York, United States, 10016 NYU Langone (...) : Choosing the Right Breast Cancer Surgery for You 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: NCT03136367 Recruitment Status : Active, not recruiting First Posted : May 2, 2017 Last Update Posted : March 6, 2019 Sponsor: Dartmouth-Hitchcock Medical Center Collaborators: Washington University School

2017 Clinical Trials

120. A Trial to Evaluate the Efficacy and Safety of Two Concentrations of VBP-926 Solution for the Treatment of Chemotherapy-associated Paronychia in Cancer Patients

using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03207906 Locations Layout table for location information United States, California Compassionate Cancer Care Fountain Valley, California, United States, 92708 United States, Illinois Northwestern University Department of Dermatology Chicago, Illinois, United States, 60611 United States, Missouri Washington University Saint Louis, Missouri, United States, 63130 (...) . Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03207906 Recruitment Status : Completed First Posted : July 5, 2017 Last Update Posted : January 25, 2019 Sponsor: Veloce BioPharma LLC Information provided by (Responsible Party): Veloce BioPharma LLC Study Details Study Description Go to Brief Summary: Paronychia is inflammation of the skin surrounding the nail that leads to secondary infection. Iatrogenic paronychia has been clearly associated with cancer chemotherapies

2017 Clinical Trials

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