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Perspectives in Clinical Research

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2016| July-September  | Volume 7 | Issue 3  

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How informed are our subjects? p. 109
Ravindra B Ghooi
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Reporting of adverse events for marketed drugs: Need for strengthening safety database p. 111
Aditi Anand Apte
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Emerging role of bioinformatics tools and software in evolution of clinical research p. 115
Supreet Kaur Gill, Ajay Francis Christopher, Vikas Gupta, Parveen Bansal
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Comparison of good clinical practice compliance and readability ease of the informed consents between observational and interventional clinical studies in the Emirates p. 123
Satish Chandrasekhar Nair, Halah Ibrahim, Omar Sherif Askar
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Assessment of adherence to the statistical components of consolidated standards of reporting trials statement for quality of reports on randomized controlled trials from five pharmacology journals p. 128
Sachin Satpute, Manthan Mehta, Sandeep Bhete, Dnyneshwar Kurle
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Assessment and classification of protocol deviations p. 132
Ravindra Bhaskar Ghooi, Neelambari Bhosale, Reena Wadhwani, Pathik Divate, Uma Divate
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Challenges in recruitment and retention of clinical trial subjects p. 137
Rashmi Ashish Kadam, Sanghratna Umakant Borde, Sapna Amol Madas, Sundeep Santosh Salvi, Sneha Saurabh Limaye
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Common pitfalls in statistical analysis: Intention-to-treat versus per-protocol analysis p. 144
Priya Ranganathan, CS Pramesh, Rakesh Aggarwal
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Single-versus double-masking in glaucoma clinical trials p. 147
DL DeMill, Barbara M Wirostko, Lindsay A Nelson, Jeanette A Stewart, William C Stewart
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