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431 results for

Saint Louis University Mental Status

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421. A Study of Patients Who Develop HIV Infection After Enrolling in HIV Vaccine Trials or HIV Vaccine Preparedness Trials

, Maryland, United States, 21201 Jhu-Cir/Dc Baltimore, Maryland, United States, 21205 Johns Hopkins Univ Baltimore, Maryland, United States, 21205 United States, Massachusetts Fenway Community Health Boston, Massachusetts, United States, 02115 Harvard University / Brigham and Women's Hospital Boston, Massachusetts, United States, 02115 United States, Missouri Saint Louis University School of Medicine Saint Louis, Missouri, United States, 63110 United States, New York New York Blood Ctr / Union Square New (...) number of saved studies (100). Please remove one or more studies before adding more. A Study of Patients Who Develop HIV Infection After Enrolling in HIV Vaccine Trials or HIV Vaccine Preparedness Trials 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: NCT00029913 Recruitment Status : Completed First

2002 Clinical Trials

422. T4N5 Liposome Lotion Compared With Placebo Lotion for Preventing Actinic Keratoses in Patients With Xeroderma Pigmentosum

Medical School Minneapolis, Minnesota, United States, 55455 United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110 United States, New York State University of New York Health Sciences Center - Stony Brook Stony Brook, New York, United States, 11790-9832 United States, Texas University of Texas - MD Anderson Cancer Center Houston, Texas, United States, 77030 United States, Washington Office of Gerald Bernstein Seattle, Washington, United States (...) number of saved studies (100). Please remove one or more studies before adding more. T4N5 Liposome Lotion Compared With Placebo Lotion for Preventing Actinic Keratoses in Patients With Xeroderma Pigmentosum 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: NCT00002811 Recruitment Status : Unknown Verified

1999 Clinical Trials

423. Depression and Health Outcomes in Refractory Epilepsy

provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00026637 Locations Layout table for location information United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110 United States, New York Columbia University Medical Center New York, New York, United States, 10032 Sponsors and Collaborators Columbia University National Institute of Neurological Disorders and Stroke (NINDS) Investigators Layout (...) Epilepsy 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: NCT00026637 Recruitment Status : Completed First Posted : November 15, 2001 Last Update Posted : November 6, 2017 Sponsor: Columbia University Collaborator: National Institute of Neurological Disorders and Stroke (NINDS) Information provided

2001 Clinical Trials

424. Long Term Interferon for Patients Who Did Not Clear Hepatitis C Virus With Standard Treatment

Massachusetts General Hospital Boston, Massachusetts, United States, 02114 UMass Memorial HealthCare, University Campus Worcester, Massachusetts, United States, 01655 United States, Michigan University of Michigan Ann Arbor, Michigan, United States, 48109 United States, Missouri Saint Louis University Saint Louis, Missouri, United States, 63104 United States, Texas University of Texas Southwestern - Dallas Dallas, Texas, United States, 75390-9195 United States, Virginia Medical College of Virginia Richmond (...) Peritonitis [ Time Frame: 1400 days (3.85 years) post randomization ] Any episode of spontaneous ascitic infection diagnosed on the basis of elevated neutrophil count (> 250/ml) in paracentesis fluid or positive bacterial cultures and clinical diagnosis in the absence of white blood cell (WBC) availability. Hepatic Encephalopathy [ Time Frame: 1400 days (3.85 years) post randomization ] Any mental status alteration which is deemed by the investigator to be due to portosystemic encephalopathy, whether

2000 Clinical Trials

425. Effect of Interleukin-2 on HIV Treatment Interruption

CRS Los Angeles, California, United States Stanford CRS Palo Alto, California, United States, 943055107 Santa Clara Valley Med. Ctr. San Jose, California, United States San Mateo County AIDS Program San Mateo, California, United States, 943055107 United States, Illinois Rush Univ. Med. Ctr. ACTG CRS Chicago, Illinois, United States, 60612 United States, Minnesota University of Minnesota, ACTU Minneapolis, Minnesota, United States, 55455 United States, Missouri Washington U CRS Saint Louis (...) Interruption 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: NCT00015704 Recruitment Status : Completed First Posted : August 31, 2001 Last Update Posted : May 22, 2012 Sponsor: National Institute of Allergy and Infectious Diseases (NIAID) Information provided by (Responsible Party): National Institute

2001 Clinical Trials

426. Radiation Therapy With or Without Chemotherapy in Treating Patients With Advanced Cancer of the Larynx

of entry) WBC at least 3,500 Platelets at least 100,000 Hepatic: Not specified Renal: (obtained within 2 weeks of entry) Creatinine clearance at least 50 mL/min (measured or calculated) Serum calcium normal Cardiovascular: Status adequate to tolerate all protocol therapy Pulmonary: Status adequate to tolerate all protocol therapy Other: Nutritional status adequate to tolerate all protocol therapy Mental status adequate to follow instructions and keep appointments No second malignancy except (...) Louis Park, Minnesota, United States, 55416 United States, New Jersey Veterans Affairs Medical Center - East Orange East Orange, New Jersey, United States, 07018-1095 CCOP - Northern New Jersey Hackensack, New Jersey, United States, 07601 United States, Ohio Ireland Cancer Center Cleveland, Ohio, United States, 44106-5065 United States, Pennsylvania Hahnemann University Hospital Philadelphia, Pennsylvania, United States, 19102-1192 University of Pittsburgh Cancer Institute Pittsburgh, Pennsylvania

1999 Clinical Trials

427. Treatment Outcome of Vascular Depression

to this study by its ClinicalTrials.gov identifier (NCT number): NCT00045773 Locations Layout table for location information United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110 United States, North Carolina Duke University Medical Center Durham, North Carolina, United States, 27710 Sponsors and Collaborators University of Pennsylvania National Institute of Mental Health (NIMH) Duke University Investigators Layout table for investigator information (...) 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: NCT00045773 Recruitment Status : Completed First Posted : September 11, 2002 Last Update Posted : October 31, 2017 Sponsor: University of Pennsylvania Collaborators: National Institute of Mental Health (NIMH) Duke University Information provided by (Responsible Party): Yvette Sheline, University

2002 Clinical Trials

428. Gabapentin For the Control of Hot Flashes in Women With Breast Cancer

, United States, 67214-3882 United States, Michigan CCOP - Kalamazoo Kalamazoo, Michigan, United States, 49007-3731 United States, Minnesota CCOP - Metro-Minnesota Saint Louis Park, Minnesota, United States, 55416 United States, New Jersey CCOP - Northern New Jersey Hackensack, New Jersey, United States, 07601 United States, New York CCOP - North Shore University Hospital Manhasset, New York, United States, 11030 CCOP - Syracuse Hematology-Oncology Associates of Central New York, P.C. Syracuse, New (...) For the Control of Hot Flashes in Women With Breast Cancer 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: NCT00022074 Recruitment Status : Completed First Posted : January 27, 2003 Last Update Posted : October 15, 2015 Sponsor: Gary Morrow Collaborator: National Cancer Institute (NCI) Information provided

2001 Clinical Trials

429. Capecitabine and Irinotecan in Treating Patients With Locally Advanced, Recurrent, or Metastatic Colorectal Cancer

Jacksonville, Florida, United States, 32209 United States, Kentucky Markey Cancer Center at University of Kentucky Chandler Medical Center Lexington, Kentucky, United States, 40536-0084 United States, Missouri St. Louis University Hospital Cancer Center Saint Louis, Missouri, United States, 63110-0250 United States, New York Lincoln Medical and Mental Health Center Bronx, New York, United States, 10451 HemOnCare, P.C. Brooklyn, New York, United States, 11235 United States, Pennsylvania Kimmel Cancer Center (...) of saved studies (100). Please remove one or more studies before adding more. Capecitabine and Irinotecan in Treating Patients With Locally Advanced, Recurrent, or Metastatic Colorectal Cancer 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: NCT00022698 Recruitment Status : Completed First Posted : January

2001 Clinical Trials

430. Collaborative Tinnitus Research at Washington University

identifier (NCT number): NCT00567892 Locations Layout table for location information United States, Missouri Washington University Medical Center Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators Washington University School of Medicine National Institute on Deafness and Other Communication Disorders (NIDCD) Investigators Layout table for investigator information Principal Investigator: Jay F Piccirillo, MD, CPI Washington University School of Medicine More Information Go (...) at Washington University (CTRWU) 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: NCT00567892 Recruitment Status : Completed First Posted : December 5, 2007 Results First Posted : August 27, 2012 Last Update Posted : November 16, 2018 Sponsor: Washington University School of Medicine Collaborator: National

2007 Clinical Trials

431. Comparison of the Saint Louis University mental status examination and the mini-mental state examination for detecting dementia and mild neurocognitive disorder--a pilot study. (PubMed)

Comparison of the Saint Louis University mental status examination and the mini-mental state examination for detecting dementia and mild neurocognitive disorder--a pilot study. The Mini-Mental State Examination (MMSE) is commonly used as a screening tool to detect dementia. However, it performs poorly in identifying persons with mild neurocognitive disorder. The Saint Louis University Mental Status (SLUMS) examination is a 30-point screening questionnaire that tests for orientation, memory (...) , attention, and executive functions.The objective of this study was to compare SLUMS and the MMSE for detecting dementia and mild neurocognitive disorder (MNCD) using Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria.Patients at the Veterans' Affairs Geriatric Research, Education and Clinical Center, St. Louis, MO (N = 702) were clinically classified as having normal cognitive functioning, MNCD, or dementia based on DSM-IV criteria. The SLUMS and MMSE were

2006 The American Journal of Geriatric Psychiatry

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