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101. Bayesian Adaptive Designs for Phase I Trials

102. Estimation and Hypothesis Testing

103. Noninferiority Trials

106. N-of-1 Randomized Trials

107. Diagnostic Trials

108. Sequential, Multiple Assignment, Randomized Trials (SMART)

109. Designs to Detect Disease Modification

110. Cross-over Trials

111. Use of Historical Data in Design

113. Device Trials

114. Randomized Selection Designs

115. Biomarker-Guided Trials

116. Platform Trial Designs

117. Factorial Trials

118. Patient-Reported Outcomes

119. Randomized Discontinuation Trials

120. Within Person Randomized Trials

121. Interim Analysis in Clinical Trials

122. Middle Development Trials

123. Futility Designs

124. Dose-Finding and Dose-Ranging Studies

125. Dose Finding for Drug Combinations

126. Outcomes in Clinical Trials

127. Translational Clinical Trials

128. Inferential Frameworks for Clinical Trials

129. Variance Control Procedures

130. Good Clinical Practice

137. Funding Models and Proposals

138. Training the Investigatorship

139. Consent Forms and Procedures

140. Contracts and Budgets

141. Data and Safety Monitoring and Reporting

142. Evolution of Clinical Trials Science

144. Multicenter and Network Trials

147. Implementing the Trial Protocol

150. Social and Scientific History of Randomized Controlled Trials

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