What proportion of ethically approved randomised clinical trials can be found in a trial registry? за авторством Speich, B, Gryaznov, D, Gloy, V, McCord, K, Agarwal, A, Kasenda, B, Briel, M

Current use and costs of electronic health records for clinical trial research: a descriptive study за авторством Mc Cord, K, Hannah, E, Ladanie, A, Briel, M, Speich, B, Bucher, H, Hemkens, L

Reporting transparency and completeness in trials: Paper 4 - reporting of randomised controlled trials conducted using routinely collected electronic records – room for improvement... за авторством McCall, SJ, Imran, M, Hemkens, LG, Mc Cord, K, Kwakkenbos, L, Sampson, M, Jawad, S, Zwarenstein, M, Relton, C, Langan, SM, Moher, D, Fröbert, O, Thombs, BD, Gale, C, Juszczak, E

Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation за авторством Speich, B, Schur, N, Gryaznov, D, Von Niederhäusern, B, Hemkens, L, Schandelmaier, S, Amstutz, A, Kasenda, B, Pauli-Magnus, C, Ojeda-Ruiz, E, Tomonaga, Y, McCord, K, Nordmann, A, Von Elm, E, Briel, M, Schwenkglenks, M, MARTA Study Group, ASPIRE Study Group

Protocol for the development of a CONSORT extension for RCTs using cohorts and routinely collected health data за авторством Kwakkenbos, L, Juszczak, E, Hemkens, L, Sampson, M, Fröbert, O, Relton, C, Gale, C, Zwarenstein, M, Langan, S, Moher, D, Boutron, I, Ravaud, P, Campbell, M, Mc Cord, K, Van Staa, T, Thabane, L, Uher, R, Verkooijen, H, Benchimol, E, Erlinge, D, Sauvé, M, Torgerson, D, Thombs, B

Protocol for the development of a CONSORT extension for RCTs using cohorts and routinely collected health data за авторством Kwakkenbos, L, Juszczak, E, Hemkens, L, Sampson, M, Fröbert, O, Relton, C, Gale, C, Zwarenstein, M, Langan, S, Moher, D, Boutron, I, Ravaud, P, Campbell, M, Mc Cord, K, van Staa, T, Thabane, L, Uher, R, Verkooijen, H, Benchimol, E, Erlinge, D, Sauvé, M, Torgerson, D, Thombs, B

Protocol for a scoping review to support development of a CONSORT extension for randomised controlled trials using cohorts and routinely collected health data за авторством Kwakkenbos, L, Imran, M, McCord, K, Sampson, M, Fröbert, O, Gale, C, Hemkens, L, Langan, S, Moher, D, Relton, C, Zwarenstein, M, Benchimol, E, Boutron, I, Campbell, M, Erlinge, D, Jawad, S, Ravaud, P, Rice, D, Sauve, M, Van Staa, T, Thabane, L, Uher, R, Verkooijen, H, Juszczak, E, Thombs, B