Table 2.
 Assessment of quality criteria for trials reporting on stenting versus no stenting after ureteroscopic retrieval of stones
| Study | Allocation concealment | Intention to treat analysis | Completeness of follow-up | Blinding* |
|---|---|---|---|---|
| Borborogluw3 | Adequate | Six participants randomised to group without stents removed from protocol and analysis because of intraoperative injury | Reported | N/A |
| Byrnew4 | N/A | N/A | Reported | N/A |
| Chenw5 | Adequate | N/A | Reported | N/A |
| Cheungw6 | Inadequate | N/A | Reported | N/A |
| Damianow2 | Adequate | N/A | Reported | N/A |
| Denstedtw1 | Adequate | 13 participants excluded from study because of intraoperative balloon dilatation | Reported | N/A |
| Jeongw7 | N/A | N/A | Reported | N/A |
| Nettow8 | N/A | N/A | Reported | Surgeon |
| Srivastavaw9 | Adequate | N/A | Reported | N/A |
N/A=not available (insufficient information provided).
*None of the trials provided sufficient information to determine blinding of participants or outcome assessors.