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Clinical Trials Design in Operative and Non Operative Invasive Procedures

https://libcat.nshealth.ca/en/permalink/provcat41736
Kamal M.F. Itani, Domenic J. Reda, editors. --Cham: Springer , 2017.
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Location
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The aim of this text is to provide the framework for building a clinical trial as it pertains to operative and non operative invasive procedures, how to get it funded and how to conduct such a trial up to publication of results. The text provides all details of building a scientifically and ethically valid proposal, including how to build the infrastructure for a clinical trial and how to move it forward through various funding agencies. The text also presents various types of clinical trials, …
Available Online
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Other Authors
Itani, Kamal M.F
Reda, Domenic J
Responsibility
Kamal M.F. Itani, Domenic J. Reda, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xxiv, 495 pages) : 42 illus., 27 illus. in color
ISBN
9783319538778
9783319538761 (print ed.)
Subjects (MeSH)
Clinical Trials as Topic
Surgical Procedures, Operative
Abstract
The aim of this text is to provide the framework for building a clinical trial as it pertains to operative and non operative invasive procedures, how to get it funded and how to conduct such a trial up to publication of results. The text provides all details of building a scientifically and ethically valid proposal, including how to build the infrastructure for a clinical trial and how to move it forward through various funding agencies. The text also presents various types of clinical trials, the use of implantable devices and FDA requirements, and adjuncts to clinical trials and interaction with industry. Clinical Trials Design in Invasive Operative and Non Operative Procedures will be of interest to all specialists of surgery, anesthesiologists, interventional radiologists, gastroenterologists, cardiologists, and pulmonologists.
Contents
Part I: Basic Principles -- The Research Question and the Hypothesis -- Primary and Secondary Endpoints -- Intervention and Control Groups -- Subject Selection -- Part II: Study Designs -- Clinical Phases of Device and Drug Evaluation with Emphasis on Early Phase Trials -- Overview of Randomized Clinical Trial and the Parallel Group Design -- Non-Inferiority and Equivalence Trials -- Factorial Designs -- Cross-over Trials -- Cluster-Randomized Clinical Trials -- Adaptive Trial Designs -- Pragmatic Trials -- Point of Care Clinical Trials -- Part III: Statistical Considerations -- Basic Statistical Considerations -- Methods and Testing of Randomization -- Sample Size Calculation -- Principles of Analysis -- Advanced Statistical Methods -- Missing Data -- Interim Monitoring -- Part IV: Ethical Considerations in Clinical Trials -- IRB and Review Process for Multisite Trials -- Trial Advertising -- Payment to Research Participants -- Conflict of Interest -- Part V: Considerations Specific to Surgical or Procedural Trials -- Quality Control in Procedural Studies -- Pilot Studies -- Surgeon Training and the Learning Curve -- Using a Placebo or Sham Procedure as a Control: Ethics and Practicalities -- Patient Recruitment and Retention in Procedural Trials -- Equipoise in Interventional Trials -- Part VI: Regulatory Considerations -- Setting up a Clinical Trial Research Office -- Regulatory Considerations: The Clinical Research Coordinator -- Data Collection Forms -- Data Security -- Remote Monitoring of Data Quality -- Investigators Meetings -- Site Visits -- Data Safety Monitoring Board: Composition and Role -- Endpoints Committee -- Regulatory Issues with Devices in Clinical Trials -- Trial Registration and Public Access to Data -- Part VII: Common Errors -- Mistakes in Clinical Trials -- Part VIII: Adjuncts to Clinical Trials -- Combined Drugs and Procedure Trials -- Genomics in Clinical Trials -- Biomarkers as Adjuncts to Clinical Trials -- Patient-centered Designs (and Outcomes) -- Economic Evaluations -- Telemedicine and Mobile Technology -- Part IX: Budgeting -- Budgeting for a Clinical Trial -- Part X: Funding -- Funding a Clinical Trial -- Writing Your Grant for the Patient Centered Outcomes Research Institute (PCORI) -- Designing Clinical Trials for Quality and Impact: The Department of Veterans Affairs Approach to Developing a Cooperative Study -- Part XI: Publication -- Publication.
Format
e-Book
Location
Online
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Pharmacotherapy of depression

https://libcat.nshealth.ca/en/permalink/provcat30376
edited by Domenic A. Ciraulo, Richard Irwin Shader. --Totowa, NJ: Springer Science+Business Media , c2011.
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Location
Online
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Author
Ciraulo, Domenic A
Other Authors
Shader, Richard Irwin
Responsibility
edited by Domenic A. Ciraulo, Richard Irwin Shader
Place of Publication
Totowa, NJ
Publisher
Springer Science+Business Media
Date of Publication
c2011
ISBN
9781603274357
Subjects (MeSH)
Depression - drug therapy
Antidepressive Agents - therapeutic use
Subjects (LCSH)
Psychiatry
Psychopharmacology
Format
e-Book
Location
Online
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Pharmacotherapy of depression

https://libcat.nshealth.ca/en/permalink/provcat21366
(2nd ed.) --New York, NY: Humana Press , 2011.
Call Number
WM 171 C578p 2011
Location
Nova Scotia Hospital
Call Number
WM 171 C578p 2011
Other Authors
Ciraulo, Domenic
Shader, Richard Irwin
Edition
2nd ed.
Place of Publication
New York, NY
Publisher
Humana Press
Date of Publication
2011
Physical Description
423 p.
ISBN
9781603274340
Subjects (MeSH)
Antidepressive Agents - therapeutic use
Depressive Disorder - drug therapy
Bipolar Disorder - drug therapy
Depression - drug therapy
Format
Book
Location
Nova Scotia Hospital
Loan Period
3 weeks
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