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Point of Maximum Impulse

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1. Point of Maximum Impulse

Point of Maximum Impulse Point of Maximum Impulse Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Point of Maximum Impulse Point (...) of Maximum Impulse Aka: Point of Maximum Impulse , Apical Thrust , Displaced Cardiac Apex , PMI From Related Chapters II. Mechanism Heart apex rotates forward with systole III. Normal impulse location Fifth intercostal space Left of mid- by 7 to 9 cm Medial to left midclavicular line by 1-2 cm IV. Accentuated Impulse Findings suggestive of Impulse > 3 cm diameter (stethoscope diaphragm size) Patient in Left Lateral Decubitus Palpation of apex Accuracy (Compared with ) Sensitivity: 92% : 91% Reference

2018 FP Notebook

2. Point of Maximum Impulse

Point of Maximum Impulse Point of Maximum Impulse Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Point of Maximum Impulse Point (...) of Maximum Impulse Aka: Point of Maximum Impulse , Apical Thrust , Displaced Cardiac Apex , PMI From Related Chapters II. Mechanism Heart apex rotates forward with systole III. Normal impulse location Fifth intercostal space Left of mid- by 7 to 9 cm Medial to left midclavicular line by 1-2 cm IV. Accentuated Impulse Findings suggestive of Impulse > 3 cm diameter (stethoscope diaphragm size) Patient in Left Lateral Decubitus Palpation of apex Accuracy (Compared with ) Sensitivity: 92% : 91% Reference

2015 FP Notebook

3. Validity of Fractional Exhaled Nitric Oxide and Impulse Oscillometry in Patients With Cough Variant Asthma

Validity of Fractional Exhaled Nitric Oxide and Impulse Oscillometry in Patients With Cough Variant Asthma Validity of Fractional Exhaled Nitric Oxide and Impulse Oscillometry in Patients With Cough Variant Asthma - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) ). Please remove one or more studies before adding more. Validity of Fractional Exhaled Nitric Oxide and Impulse Oscillometry in Patients With Cough Variant Asthma 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: NCT03573284

2018 Clinical Trials

4. Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD

Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies (...) before adding more. Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With ADHD 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: NCT03638466 Recruitment Status : Not yet recruiting First Posted

2018 Clinical Trials

5. Effects of tDCS on Impulsiveness Among People Suffering From Borderline Personality Disorder

Effects of tDCS on Impulsiveness Among People Suffering From Borderline Personality Disorder Effects of tDCS on Impulsiveness Among People Suffering From Borderline Personality Disorder - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more (...) of the BIS-10 is a self-rated 34 item questionnaire, composed by three subscales: motor-impulsivity, cognitive-impulsivity and non-planning-impulsivity. Each item is scored on a 0 to 4 points scale. Higher scores indicate higher levels of impulsivity. HDRS scores [ Time Frame: Baseline (Day 0), Day 5, Day 12 and Day 30 post-tDCS ] Compared scores from the Hamilton Depression Rating Scale (HDRS). The HDRS is a clinician-rated 17 item scale which allows depression severity assessment and follow-up. Each

2018 Clinical Trials

6. Treating Impulsivity in Adults With Probiotics

Treating Impulsivity in Adults With Probiotics Treating Impulsivity in Adults With Probiotics - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Treating Impulsivity in Adults With Probiotics (PROBIA (...) at weeks 10, and 20. ] assessed by the Adult Attention-Deficit/Hyperactivity Disorder Rating Scale (ADHD-RS). The ADHD-RS is a 18-items scale self-report version for assessing symptoms for ADHD DSM-IV. It consists of a subscale of inattention (IN, 9-items), another of hyperactivity/impulsivity (H / I, 9-items) and the total (TOT, 18-items). The interviewees are asked about the frequency of the symptoms over the past 6 months. Each item is scored from 0 to 3 points, and the highest scores indicates more

2018 Clinical Trials

7. Study of Clonidine Efficacy for the Treatment of Impulse Control Disorders in Parkinson's Disease:

Study of Clonidine Efficacy for the Treatment of Impulse Control Disorders in Parkinson's Disease: Study of Clonidine Efficacy for the Treatment of Impulse Control Disorders in Parkinson's Disease: - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove (...) . Diminution of impulse control disorder severity on the initial more elevated sub-score of the QUIP-RS between the first visit and the eighth week under clonidine. Secondary Outcome Measures : MDS-UPDRS [ Time Frame: at 4 and 8 weeks ] The Movement Disorder Society Unified Parkinson Disease Rating STAI [ Time Frame: at 4 and 8 weeks ] State-Trait Anxiety Index BDI II [ Time Frame: at 4 and 8 weeks ] Beck Depression Inventory II It is a self-administered questionnaire each of them using a four-point

2018 Clinical Trials

8. The Effect of Mindfulness-based Relapse Prevention on Impulsive Control Circuit Among Methamphetamine Dependents

The Effect of Mindfulness-based Relapse Prevention on Impulsive Control Circuit Among Methamphetamine Dependents The Effect of Mindfulness-based Relapse Prevention on Impulsive Control Circuit Among Methamphetamine Dependents - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) Measures Go to Primary Outcome Measures : craving change [ Time Frame: change from baseline, 4,8,12,27and 52 weeks ] craving will be measured by visual analogue scale(VAS), participants specify their level of craving by indicating a position along a continuous line between two end-points, score ranges from 0 to 10, 0 refers to the lowest level of craving, 10 refers to the highest level of craving impulsiveness change [ Time Frame: baseline,4,8,12,27and 52 weeks ] impulsiveness will be measured

2018 Clinical Trials

9. Effects of Mindfulness Training on Emotion Regulation and Impulsivity

Effects of Mindfulness Training on Emotion Regulation and Impulsivity Effects of Mindfulness Training on Emotion Regulation and Impulsivity - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Effects (...) was focused on improving interpersonal effectiveness. Outcome Measures Go to Primary Outcome Measures : Difficulties in Emotion Regulation Scale (DERS) [ Time Frame: 1-past week ] The DERS is a 28-item-scale that measures difficulties in emotion regulation. Each item has to be rated in a 5-point scale, with higher scores indicating higher difficulties in emotion regulation. Barrat Impulsiveness Scale (BIS-11) [ Time Frame: 1-past week ] The current version of the Barratt Impulsiveness Scale is composed

2017 Clinical Trials

10. Modulating Impulsivity in Suicidal Adolescents With tDCS

Modulating Impulsivity in Suicidal Adolescents With tDCS Modulating Impulsivity in Suicidal Adolescents With tDCS - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Modulating Impulsivity in Suicidal (...) provided by (Responsible Party): Richard Liu, Lifespan Study Details Study Description Go to Brief Summary: As a first step toward investigating whether modulation of impulsivity and associated neural pathways may yield clinically meaningful changes in risk for adolescent suicidal behavior, the R21 is a proof-of concept study evaluating the potential for tDCS targeting brain regions associated with behavioral impulsivity (right inferior frontal gyrus [rIFG]) and cognitive impulsivity (left

2017 Clinical Trials

11. Endovascular Crossing of Chronic Total Occlusions Using an Impulse: An Explorative Design Study (PubMed)

was evaluated by measuring the peak force and momentum for different spring compressions and strike distances in air and blood-mimicking fluid. Puncture performance, in terms of number of punctures, number of strikes to puncture, and energy transfer from the indenter to the CTO, was assessed for six tip shapes (stamp, wedge, spherical, pointed, hollow spherical, and ringed) on three CTO models with different weight percentages of gelatin and calcium. As a control, a Ø0.4 mm rigid rod was tested. A maximum (...) Endovascular Crossing of Chronic Total Occlusions Using an Impulse: An Explorative Design Study In this study we investigated whether exerting an impulse on a Chronic Total Occlusion (CTO) improves the success rate of CTO crossing as compared to the currently used method of statically pushing the guidewire against the CTO. A prototype (Ø2 mm) was developed that generates translational momentum using a spring-loaded indenter and converts it to an impulse during impact. Mechanical performance

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2017 Cardiovascular engineering and technology

12. Neurokinin (NK) 1 Antagonist for Pathological Aggression for Harmful, Impulsive, and Self-/Aggressive Behaviour

Neurokinin (NK) 1 Antagonist for Pathological Aggression for Harmful, Impulsive, and Self-/Aggressive Behaviour Neurokinin (NK) 1 Antagonist for Pathological Aggression for Harmful, Impulsive, and Self-/Aggressive Behaviour - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved (...) studies (100). Please remove one or more studies before adding more. Neurokinin (NK) 1 Antagonist for Pathological Aggression for Harmful, Impulsive, and Self-/Aggressive Behaviour (AHIMSA-1) 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

2016 Clinical Trials

13. Nalmefene, Baclofen and Impulsivity in Subjects With Alcohol Use Disorder and Healthy Control Subjects

Nalmefene, Baclofen and Impulsivity in Subjects With Alcohol Use Disorder and Healthy Control Subjects Nalmefene, Baclofen and Impulsivity in Subjects With Alcohol Use Disorder and Healthy Control Subjects - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please (...) remove one or more studies before adding more. Nalmefene, Baclofen and Impulsivity in Subjects With Alcohol Use Disorder and Healthy Control Subjects 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: NCT03034408 Recruitment

2016 Clinical Trials

14. Fatigue strength of bovine articular cartilage-on-bone under three-point bending: the effect of loading frequency. (PubMed)

Fatigue strength of bovine articular cartilage-on-bone under three-point bending: the effect of loading frequency. The objective of this study was to determine the influence of loading frequency on the failure of articular cartilage-on-bone specimens under three-point bending.In this study, cyclic three-point bending was used to introduce failure into cartilage-on-bone specimens at varying loading frequencies. Sinusiodally varying maximum compressive loads in the range 40-130 N were applied (...) to beam-shaped cartilage-on-bone specimens at frequencies of 1, 10, 50 and 100 Hz.The number of cycles to failure decreased when loading frequency increased from normal and above gait (1 and 10 Hz) to impulsive loading frequencies (50 and 100 Hz). It was found that 67 and 27% of the specimens reached run-out at loading of 10,000 cycles at frequencies of 1 and 10 Hz, respectively. However, 0% of the specimens reached run-out at loading frequencies of 50 and 100 Hz.The results indicate that increasing

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2017 BMC Musculoskeletal Disorders

15. The Effects of Yoga on Attention, Impulsivity and Hyperactivity in Pre-school Age Children

The Effects of Yoga on Attention, Impulsivity and Hyperactivity in Pre-school Age Children The Effects of Yoga on Attention, Impulsivity and Hyperactivity in Pre-school Age Children - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more (...) studies before adding more. The Effects of Yoga on Attention, Impulsivity and Hyperactivity in Pre-school Age Children 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: NCT02642666 Recruitment Status : Completed First Posted : December 30, 2015 Last Update Posted : May 30, 2017 Sponsor: University

2015 Clinical Trials

16. Changing Impulsivity With Mindful Breathing Therapy to Reduce Problem Drinking

Changing Impulsivity With Mindful Breathing Therapy to Reduce Problem Drinking Changing Impulsivity With Mindful Breathing Therapy to Reduce Problem Drinking - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more (...) . Changing Impulsivity With Mindful Breathing Therapy to Reduce Problem Drinking (BBMT) 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: NCT02527720 Recruitment Status : Unknown Verified February 2016 by Carl W. Lejuez, University of Maryland. Recruitment status was: Recruiting First Posted : August 19, 2015

2015 Clinical Trials

17. Evaluation of Conventional Ablation With or Without Focal Impulse and Rotor Modulation to Eliminate Human AF

Evaluation of Conventional Ablation With or Without Focal Impulse and Rotor Modulation to Eliminate Human AF Evaluation of Conventional Ablation With or Without Focal Impulse and Rotor Modulation to Eliminate Human AF - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (...) (100). Please remove one or more studies before adding more. Evaluation of Conventional Ablation With or Without Focal Impulse and Rotor Modulation to Eliminate Human AF (RECONFIRM) 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

2015 Clinical Trials

18. Heroin delay discounting: modulation by pharmacological state, drug-use impulsivity and intelligence (PubMed)

influence heroin DD at short (ecologically relevant) delays during two pharmacological states (heroin satiation and withdrawal). Out-of-treatment, intensive heroin users (n = 170; 53.5% African American; 66.7% male) provided complete DD data during imagined heroin satiation and withdrawal. Delays were 3, 6, 12, 24, 48, 72, and 96 hours; maximum delayed heroin amount was thirty $10 bags. Indifference points were used to calculate area under the curve (AUC). We also assessed drug-use impulsivity (...) Heroin delay discounting: modulation by pharmacological state, drug-use impulsivity and intelligence Delay discounting (DD) refers to how rapidly an individual devalues goods based on delays to receipt. DD usually is considered a trait variable but can be state dependent, yet few studies have assessed commodity valuation at short, naturalistically relevant time intervals that might enable state-dependent analysis. This study aimed to determine whether drug-use impulsivity and intelligence

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2015 Experimental and clinical psychopharmacology

19. Monotherapy Brexpiprazole (OPC-34712) Trial in the Treatment of Adults With Schizophrenia With Impulsivity

Monotherapy Brexpiprazole (OPC-34712) Trial in the Treatment of Adults With Schizophrenia With Impulsivity Monotherapy Brexpiprazole (OPC-34712) Trial in the Treatment of Adults With Schizophrenia With Impulsivity - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) bias. Scores were not bounded by a minimum or maximum range, higher fMRI BOLD activation scores indicate increased brain blood flow, which reflects brain activity. Change From Baseline Brain Activation in the VLPFC Based on Change From Baseline to Week 6 in fMRI BOLD Activation Score in the Right VLPFC During Performance of the SSRT Task [ Time Frame: At baseline (Day 0), and week 6 (Day 42) of the treatment phase ] To evaluate the effect of brexpiprazole on brain regions activated by impulsive

2014 Clinical Trials

20. Intraoperative Analysis of Reward and Impulsivity in the Basal Ganglia

Intraoperative Analysis of Reward and Impulsivity in the Basal Ganglia Intraoperative Analysis of Reward and Impulsivity in the Basal Ganglia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Intraoperative (...) links to impulsivity in human populations. In the balloon analogue risk task (BART) participants must balance risk and reward as they decide when to stop inflating a computerized balloon whose point value and risk of popping both grow with size. In the stop signal reaction task (SSRT), participants must respond as quickly as possible when a "go" cue appears, but countermand this response when a "stop" tone is played. At the neural level, the BART allows us to elucidate correlates of risk, outcome

2014 Clinical Trials

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