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. 2018 Nov 21;13(11):e0206296. doi: 10.1371/journal.pone.0206296

Table 3. Assessment of risk of bias for the clinical trials included.

Questions to be considered
Study Random sequence generation Allocation concealment Blinding of participants and personnel Blinding of outcome assessment Free of incomplete outcome data Free from baseline imbalance Other sources of bias
Louw et al. (2002) YES UNCLEAR NO UNCLEAR UNCLEAR UNCLEAR UNCLEAR
Taifour et al. (2002) YES UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR
Honkala et al. (2003) YES UNCLEAR NO NO UNCLEAR UNCLEAR UNCLEAR
Yu et al. (2004) YES UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR
van den Dungen et al. (2004) YES UNCLEAR NO YES UNCLEAR UNCLEAR UNCLEAR
Ersin et al. (2006) YES UNCLEAR UNCLEAR YES UNCLEAR UNCLEAR UNCLEAR
Innes et al. (2011) YES YES NO NO UNCLEAR UNCLEAR UNCLEAR
Mijan et al. (2014) YES NO NO NO UNCLEAR UNCLEAR UNCLEAR
Santamaria et al. (2014) YES YES NO NO UNCLEAR UNCLEAR UNCLEAR
Borges et al. (2012) YES YES UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR
Hesse et al. (2014) YES UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR UNCLEAR
Santos et al. (2012) YES UNCLEAR NO NO UNCLEAR UNCLEAR UNCLEAR
Zhi et al. (2012) YES UNCLEAR UNCLEAR YES UNCLEAR YES UNCLEAR
Duangthip et al. (2016) YES UNCLEAR YES YES YES YES UNCLEAR