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Saint Louis University Mental Status

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161. Post‐Traumatic Stress Symptoms (PTSS) in Transplant Recipients

Transplantation Saint Louis, Missouri, United States, 63110 United States, New York Columbia University Medical Center: Pediatric Transplantation New York, New York, United States, 10032 United States, Ohio Cincinnati Children's Hospital Medical Center: Pediatric Transplantation Cincinnati, Ohio, United States, 45229 Nationwide Children's Hospital Columbus, Ohio, United States, 43205 United States, Pennsylvania Children's Hospital of Philadelphia: Pediatric Transplantation Philadelphia, Pennsylvania, United (...) Index (MLVI) [ Time Frame: 6 months post enrollment ] Defined by an MLVI greater than 2. Above-threshold Child PTSS Score [ Time Frame: At enrollment visit ] Defined as the existence of threshold scores in a symptoms constellation corresponding to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) definition of Post-Traumatic Stress Disorder (PTSD). Method: University of California at Los Angeles Post-Traumatic Stress Disorder Reaction Index DSM-5 version (UCLA PTSD RI

2016 Clinical Trials

162. Cerclage for Short Cervix in Twins

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: NCT02912390 Recruitment Status : Terminated (On Internal Hold) First Posted : September 23, 2016 Last Update Posted : April 13, 2018 Sponsor: St. Louis University Information provided by (Responsible Party): Laura Vricella, MD, St. Louis University Study Details Study Description Go to Brief Summary: Through cervical (...) of routine care at St. Mary's Health Center (SMHC) and Saint Louis University's (SLUCare) Physician Group. (Transvaginal cervical length measurement every 2 weeks from 16weeks/0days-23weeks/6days weeks, per hospital practice) Women pregnant with twin gestations at SMHC who meet study criteria will undergo transvaginal length screening between 16 and 24 weeks gestation. Those women with transvaginal cervical length measurements at or below 25 mm will be approached for study participation. If a patient

2016 Clinical Trials

163. Bariatric Embolization of Arteries in Obese Patients With HCC to Allow Salvage Liver Transplantation

Status : Recruiting First Posted : October 17, 2016 Last Update Posted : December 7, 2018 See Sponsor: St. Louis University Information provided by (Responsible Party): Keith Pereira, MD:, St. Louis University Study Details Study Description Go to Brief Summary: Hepatocellular carcinoma (HCC) is the most common primary malignant liver tumor and has a grave prognosis. Obesity is an epidemic in the US.Patients with HCC and obesity are not candidates for liver transplantation, depriving them of the best (...) 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): NCT02935478 Contacts Layout table for location contacts Contact: Keith Pereira, MD 314-268-5558 Locations Layout table for location information United States, Missouri Saint Louis University Recruiting Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators St. Louis University Investigators Layout table

2016 Clinical Trials

164. Shifting Rehabilitation Paradigms in Skilled Nursing Facilities

Question survey, scoring each questions on a 1-10 scale (1=not at all, 10=extremely) Saint Louis University Mental Status Exam (SLUMS) [ Time Frame: Quantification at SNF Admission (baseline/initial evaluation) ] SLUMS screens for cognitive impairments by assessing participant function in the areas of attention, calculation, immediate and delayed recall, animal naming, and visuospatial skills Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study (...) Paradigms in Skilled Nursing Facilities 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: NCT02927171 Recruitment Status : Completed First Posted : October 6, 2016 Last Update Posted : January 24, 2019 Sponsor: VA Office of Research and Development Collaborator: University of Colorado, Denver Information

2016 Clinical Trials

165. AFQ056 for Language Learning in Children With FXS

, MD, MPH United States, Missouri St Louis Children's Hospital (Washington University School of Medicine) Recruiting Saint Louis, Missouri, United States, 63110 Contact: Kathleen Black 314-362-7166 Contact: Mangesha Teshome 314-77-8420 Principal Investigator: Bryan McGill, MD, PhD United States, New York Columbia University - New York Presbyterian Recruiting New York, New York, United States, 10605 Contact: Elizabeth Aaron 914-997-5242 Principal Investigator: Jeremy Veenstra-VanderWeele, MD United (...) 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: NCT02920892 Recruitment Status : Recruiting First Posted : September 30, 2016 Last Update Posted : August 29, 2018 See Sponsor: Elizabeth Berry-Kravis Collaborator: National

2016 Clinical Trials

166. Analyzing Retinal Microanatomy in ROP

): NCT02887157 Contacts Layout table for location contacts Contact: Maureen G Mcguire, PhD 215-615-1501 Locations Layout table for location information United States, Florida University of Florida Active, not recruiting Gainesville, Florida, United States, 32611 United States, Missouri Washington University Active, not recruiting Saint Louis, Missouri, United States, 63130 United States, North Carolina Duke University Eye Center Recruiting Durham, North Carolina, United States, 27705 Contact: Cynthia A Toth (...) 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: NCT02887157 Recruitment Status : Recruiting First Posted : September 2, 2016 Last Update Posted : December 14, 2018 See Sponsor: Duke University Collaborators: National Eye Institute (NEI) University of Pennsylvania

2016 Clinical Trials

167. Bariatric Embolization of Arteries for the Treatment of Nonalcoholic Steatohepatitis

: Keith Pereira, MD 314-268-5558 Locations Layout table for location information United States, Missouri Saint Louis University Saint Louis, Missouri, United States, 63110 Sponsors and Collaborators Keith Pereira, MD: Investigators Layout table for investigator information Principal Investigator: Keith Pereira, MD Assistant professor of radiology-Interventional radiology Principal Investigator: Brent Neuschwander-Tetri, MD Professor of medicine- gastroenterology Principal Investigator: Kirubahara (...) , 2016 Last Update Posted : August 17, 2018 See Sponsor: Keith Pereira, MD: Information provided by (Responsible Party): Keith Pereira, MD:, St. Louis University Study Details Study Description Go to Brief Summary: Obesity is an epidemic in the US. With progression of obesity, Nonalcoholic steatohepatitis (NASH) has been a growing public health issue. Presently there is no cure for NASH.Prevention of progression of fibrosis in NASH is crucial, as they are at a high risk for cirrhosis and may need

2016 Clinical Trials

168. Optimizing Outcomes of Treatment-Resistant Depression in Older Adults

, California, United States, 90095 Contact: Natalie St. Cyr, MA 310-983-3375 Principal Investigator: Helen Lavretsky, MD United States, Missouri Washington University School of Medicine Healthy Mind Lab Recruiting Saint Louis, Missouri, United States, 63110 Contact: Emily Lenard, BA 314-747-5706 Contact: Julie Schweiger, BA 314-362-3153 Principal Investigator: Eric Lenze, MD United States, New York Columbia University Adult and Late Life Depression Clinic Recruiting New York, New York, United States, 10032 (...) through a Washington University in St. Louis (WUSTL) secure repository and registered at clinicaltrials.gov. Layout table for additional information Studies a U.S. FDA-regulated Drug Product: Yes Studies a U.S. FDA-regulated Device Product: No Product Manufactured in and Exported from the U.S.: No Keywords provided by Eric Lenze, Washington University School of Medicine: Comparative Effectiveness Research Pragmatic Clinical Trials Patient-Centered Outcomes Research Additional relevant MeSH terms

2016 Clinical Trials

169. Phase 4, Controlled Study in Adult Subjects Undergoing Primary, 1-2 Level, Open Lumbar Spinal Fusion Surgery

mouth, nausea, vomiting, constipation, altered mental status, pruritus, urinary retention, and postoperative ileus [ Time Frame: 30 days ] The OBAS total score at 24, 48, and 72 hours [ Time Frame: 72 hours ] Pain interference at Day 1 Pre-op and Day 14 [ Time Frame: 14 Days ] Nurse's satisfaction with overall analgesia at 24, 48, and 72 hours or upon hospital discharge [ Time Frame: 72 hours ] total opioid consumption (in IV morphine equivalents) from 0-48 hours [ Time Frame: 48 hours ] total (...) States, 95817 United States, Massachusetts Massachusetts General Hospital Boston, Massachusetts, United States, 02114 United States, Michigan Beaumont Health Troy, Michigan, United States, 48085 United States, Missouri Washington Univ Saint Louis, Missouri, United States, 63110 United States, New York Icahn School of Medicine New York, New York, United States, 10029 United States, North Carolina OrthoCarolina Charlotte, North Carolina, United States, 28207 United States, Ohio Ohio State Univ Columbus

2016 Clinical Trials

170. A Study of the Relationship of Psychosocial Function With Mood Symptoms in Offspring of Parents With Bipolar Disorder

, Indiana Indiana University Recruiting Indianapolis, Indiana, United States, 46202 United States, Maryland Johns Hopkins University School of Medicine Recruiting Baltimore, Maryland, United States, 21205 United States, Massachusetts Massachusetts General Hospital Recruiting Boston, Massachusetts, United States, 02114 United States, Michigan University of Michigan Recruiting Ann Arbor, Michigan, United States, 48109-2700 United States, Missouri Washington University Withdrawn Saint Louis, Missouri (...) . ClinicalTrials.gov Identifier: NCT03017781 Recruitment Status : Recruiting First Posted : January 11, 2017 Last Update Posted : February 11, 2019 See Sponsor: Janssen Research & Development, LLC Information provided by (Responsible Party): Janssen Research & Development, LLC Study Details Study Description Go to Brief Summary: The primary purpose of this study is to compare, over 24 months, the time spent with clinically significant mood symptoms (ie, mania, depression), as measured by the Longitudinal Interval

2016 Clinical Trials

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

United States, Georgia NeuroTrials Research Inc Atlanta, Georgia, United States, 30342 United States, Missouri St. Lukes Hospital Chesterfield, Missouri, United States, 63017 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 Investigators Layout table for investigator information Principal Investigator: Russell Rosenberg, PhD (...) 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: NCT02797678 Recruitment Status : Completed First Posted : June 13, 2016 Results First Posted : January 11, 2019 Last Update Posted : January 11, 2019 Sponsor: Philips Respironics Information provided by (Responsible Party

2016 Clinical Trials

172. Follow up 18F-AV-1451 Scan in Confirmatory Cohort Subjects From Study 18F-AV-1451-A05

Massachusetts General Hospital Boston, Massachusetts, United States, 02114 Boston University School of Medicine Boston, Massachusetts, United States, 02118 United States, Missouri Washington University School of Medicine Saint Louis, Missouri, United States, 63110 United States, Nevada Las Vegas Radiology Las Vegas, Nevada, United States, 89113 United States, New York New York University Center for Brain Health New York, New York, United States, 10016 United States, North Carolina Duke University Medical (...) for Headache Santa Monica, California, United States, 90404 United States, Florida Neuropsychiatric Research Center of Southwest Florida Fort Myers, Florida, United States, 33912 Compass Research, LLC Orlando, Florida, United States, 32806 Meridien Research Saint Petersburg, Florida, United States, 33709 University of South Florida Health Byrd Alzheimer's Institute Tampa, Florida, United States, 33613 Premiere Research Institute West Palm Beach, Florida, United States, 33407 United States, Massachusetts

2016 Clinical Trials

173. Evaluation the Efficacy of Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in the Identification of Colonic Polyps in a Screening Population.

Hospital Springfield, Massachusetts, United States, 01199 United States, Minnesota Mayo Clinic Rochester Rochester, Minnesota, United States, 55905 United States, Missouri Clinical Research Professionals Saint Louis, Missouri, United States, 63141 United States, New York NYU New York, New York, United States, 10016 Columbia University New York, New York, United States, 10032 United States, North Carolina Asheville Gastroenterology Associates Asheville, North Carolina, United States, 28801 United States (...) it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02754661 Recruitment Status : Completed First Posted : April 28, 2016 Last Update Posted : January 29, 2019 Sponsor: Medtronic - MITG Information provided by (Responsible Party): Medtronic - MITG Study Details Study Description Go to Brief Summary: The primary objective of this multicenter, prospective, randomized study is to assess the diagnostic yield of CCE versus CTC in a screening

2016 Clinical Trials

174. Nitrous TRD Bipolar Depression

information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02757521 Contacts Layout table for location contacts Contact: Britt Gott 3143622463 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Jennifer Anger 314-747-7348 Principal Investigator: Peter Nagele, MD Sponsors and Collaborators Washington University School (...) 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: NCT02757521 Recruitment Status : Recruiting First Posted : May 2, 2016 Last Update Posted : November 7, 2018 See Sponsor: Washington University School of Medicine Collaborators: Stanley Medical Research Institute PPD Information provided

2016 Clinical Trials

175. TTFields and Pulsed Bevacizumab for Recurrent Glioblastoma

States, Florida University of Florida Recruiting Gainesville, Florida, United States, 32611 Contact: David Tran, MD, PhD 352-294-8137 Principal Investigator: David D Tran, MD, PhD United States, Missouri Washington University Recruiting Saint Louis, Missouri, United States, 63110 Contact: Grayson Talcott, BS 314-273-0656 Principal Investigator: George Ansstas, M.D. Sponsors and Collaborators University of Florida NovoCure Ltd. Investigators Layout table for investigator information Principal (...) for Recurrent Glioblastoma 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: NCT02663271 Recruitment Status : Recruiting First Posted : January 26, 2016 Last Update Posted : March 14, 2019 See Sponsor: University of Florida

2016 Clinical Trials

176. The Use of Transcranial Electrical Stimulation for Hallucinations

Electrical Stimulation for Hallucinations 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: NCT02715765 Recruitment Status : Recruiting First Posted : March 22, 2016 Last Update Posted : November 27, 2017 See Sponsor: University (...) of Minnesota - Clinical and Translational Science Institute Collaborator: Minneapolis Veterans Affairs Medical Center Information provided by (Responsible Party): University of Minnesota - Clinical and Translational Science Institute Study Details Study Description Go to Brief Summary: Schizophrenia is a serious mental health disorder that affects approximately 1% of the population. Auditory hallucinations are present in as many as 50-75% of patients with this diagnosis. The hallucinations experienced

2016 Clinical Trials

177. Sleep Quality and Amyloid-Beta Kinetics

Layout table for location contacts Contact: Cristina Toedebusch, BS 314-747-0646 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63144 Contact: Cristina Toedebusch, BS 314-747-0646 Sponsors and Collaborators Washington University School of Medicine Investigators Layout table for investigator information Principal Investigator: Brendan Lucey, MD Washington University Medical School More (...) 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: NCT03077620 Recruitment Status : Recruiting First Posted : March 13, 2017 Last Update Posted : February 15, 2019 See Sponsor: Washington University School of Medicine Information provided by (Responsible Party

2016 Clinical Trials

178. Evaluating the Relationship Between Tau PET Imaging and CSF Biomarkers of AD (Alzheimer Disease) in Humans

research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03287765 Contacts Layout table for location contacts Contact: Kelley Jackson, BA 314 3621558 Contact: Theresa Butler, RN 314-362-1558 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: Kelley Jackson 314-362-1558 Sponsors (...) : NCT03287765 Recruitment Status : Recruiting First Posted : September 19, 2017 Last Update Posted : January 24, 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 purpose of this research study is to evaluate a new radioactive compound used in positron emission tomography (PET) scans in identifying tau tangles (a certain protein that might be associated

2016 Clinical Trials

179. F 18 T807 PET (Positron Emission Tomograph )Scan for HIV Infected & Uninfected

314 362-1558 Locations Layout table for location information United States, Missouri Washington University School of Medicine Recruiting Saint Louis, Missouri, United States, 63110 Contact: John Doyle, BA, MA 314-747-1072 Sub-Investigator: Beau Ances, MD, PhD Sponsors and Collaborators Washington University School of Medicine Investigators Layout table for investigator information Principal Investigator: Tammie Benzinger, MD, PhD Washington University School of Medicine More Information Go (...) . F 18 T807 PET (Positron Emission Tomograph )Scan for HIV Infected & Uninfected 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: NCT03279523 Recruitment Status : Recruiting First Posted : September 12, 2017 Last Update

2016 Clinical Trials

180. Inhaled Nitrous Oxide for Treatment-Resistant Depression: Optimizing Dosing Strategies

-2463 Contact: Linda Barnes 314-747-7348 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 314-362-2463 Contact: Linda Barnes 314-747-7348 Principal Investigator: Peter Nagele, MD Sponsors and Collaborators Washington University School of Medicine Brain & Behavior Research Foundation Investigators Layout table for investigator information Principal (...) : There is no plan to share IPD. Keywords provided by Ben Palanca, Washington University School of Medicine: Depression treatment-resistant Additional relevant MeSH terms: Layout table for MeSH terms Disease Depression Depressive Disorder Depressive Disorder, Treatment-Resistant Depressive Disorder, Major Pathologic Processes Behavioral Symptoms Mood Disorders Mental Disorders Anesthetics Nitrous Oxide N-Methylaspartate Central Nervous System Depressants Physiological Effects of Drugs Anesthetics, Inhalation

2016 Clinical Trials

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