| Methods | Randomised, parallel group study. Patients and outcome assessor blind. No withdrawals. | |
| Participants | Adults. Age 35 to 65 years. 20 enrolled and results given for 20. | |
| Interventions | 2 groups. Antiseptic mouthwash (20 ml Listerine) rinse twice per day for 30 seconds versus placebo (5% hydroalcohol). Recall every month. Study duration: 3 months. | |
| Outcomes | Turesky modification of Quigley‐Hein plaque index, a modification of the Ainamo and Bay bleeding index, probing attachment levels (mm), probing pocket depth (mm) at 1, 2, 3 months. 3‐month data used. | |
| Notes | The Ainamo and Bay bleeding index was recorded using a "sweeping motion" and not with a "gentle probing". | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | "Subjects were then assigned by a computer‐ generate random code to one of two mouthrinse groups". |
| Allocation concealment (selection bias) | Low risk | "All mouthrinse bottles were coded and neither the examiner, individual dispensing mouthrinses, nor subjects were aware of treatment code". |
| Blinding (performance bias and detection bias) All outcomes | Low risk | "All mouthrinse bottles were coded and neither the examiner, individual dispensing mouthrinses, nor subjects were aware of treatment code". |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | All data reported. No loss to follow‐up. |
| Selective reporting (reporting bias) | Low risk | All data reported. |
| Other bias | Low risk | |
| Blinding of the patient? | Low risk | "All mouthrinse bottle were coded and neither the examiner, individual dispensing mouthrinses, nor subjects were aware of treatment code". |