Table 2.
Criteria | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Studies | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | Total |
Clear aim | Inclusion of consecutive patients | Prospective data collection | Endpoints appropriate to the aim | Unbiased assessment of the endpoint | Follow-up period appropriate | Follow-up loss less than 5% | Prospective calculation of the study size | Adequate control group | Contemporary groups | Baseline equivalence of groups | Adequate statistical analyses | ||
Fränkel and Fränkel (30) | 1 | 0 | 0 | 2 | 0 | 2 | 2 | 0 | 2 | 0 | 0 | 1 | 10 |
Haydar and Enacar (33) | 2 | 0 | 0 | 2 | 0 | 2 | 2 | 0 | 2 | 0 | 2 | 2 | 14 |
Cozza et al. (12) | 2 | 2 | 2 | 2 | 0 | 2 | 2 | 1 | 2 | 1 | 2 | 2 | 20 |
Defraia et al. (14) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 2 | 2 | 16 |
Weinbach and Smith (37) | 2 | 1 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 2 | 0 | 2 | 16 |
Freeman et al. (15) | 2 | 1 | 1 | 2 | 0 | 2 | 2 | 1 | 2 | 1 | 2 | 2 | 18 |
Barbre and Sinclair (32) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 1 | 2 | 15 |
Kuster and Ingervall (35) | 2 | 1 | 0 | 2 | 0 | 2 | 0 | 0 | 2 | 2 | 1 | 1 | 13 |
Işcan et al. (34) | 2 | 0 | 0 | 2 | 0 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | 10 |
Işcan and Sarisoy (40) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 2 | 2 | 2 | 17 |
Bazzucchi et al. (41) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 1 | 2 | 15 |
Albogha et al. (25) | 2 | 2 | 2 | 2 | 0 | 2 | 2 | 1 | 2 | 2 | 2 | 2 | 21 |
Sankey et al. (42) | 2 | 1 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 2 | 2 | 17 |
Baccetti et al. (16) | 2 | 1 | 1 | 2 | 2 | 2 | 2 | 1 | 2 | 1 | 2 | 2 | 20 |
Schulz et al. (45) | 2 | 1 | 1 | 2 | 0 | 2 | 2 | 1 | 2 | 1 | 2 | 2 | 18 |
Cinsar et al. (11) | 2 | 0 | 0 | 2 | 0 | 2 | 2 | 0 | 2 | 0 | 2 | 2 | 14 |
Jacob et al. (24) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 2 | 2 | 16 |
Ngan et al. (36) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 2 | 2 | 16 |
Işcan et al. (43) | 2 | 0 | 1 | 2 | 0 | 2 | 2 | 0 | 2 | 1 | 2 | 2 | 16 |
nRCT, non-randomized clinical trial.