Publication | Design | Population | Case definition | Period | Test | Control | Mean (SD) outcome |
---|---|---|---|---|---|---|---|
Schenk et al. [16] | RCT Split-mouth design | 8 patients | PD >4 mm BOP on at least 1 site per implant ± mucosal hyperplasia no radiographic bone loss | 3 months | Supra-/subgingival scaling (steel curettes) + polishing (rubber cup) + locally delivered tetracycline HCl (25 %) fibre for 10 days +0.2 % CHX mouthrinse twice for 10 days | Supra-/subgingival scaling (steel curettes) + polishing (rubber cup) + +0.2 % CHX mouthrinse twice for 10 days | ΔBOP (3 months, subject level) |
 |  | 24 implants |  |  |  |  | Test: −17 ± 25 % |
 |  | 1 implant type (endossous part: titanium and zirconoxide/transmucosal part: titanium oxinitride) |  |  |  |  | Control: 15 ± 37 % |
 |  |  |  |  |  |  | PD/CAL values without significant changes in both groups |
 |  |  |  |  |  |  | No adverse events |
 |  |  |  |  |  |  | Partial/complete fibre loss at three sites |
Hallström et al. [19] | RCT, parallel | 45 patients | PD ≥4 mm BOP + and/or pus | 6 months | OHI + mechanical cleansing (titanium curettes + rubber cups + polishing paste) + Azithromycin® 500 mg day 1 and 250 mg days 2–4 | OHI + mechanical cleansing (titanium curettes + rubber cups + polishing paste) | Test |
 |  | 3 implant systems | Radiographic bone loss ≤2 mm |  |  |  | BOP: 82.6 (24.4) (BL) to 27.3 (18.8) % (6 months, subject level) |
 |  |  |  |  |  |  | PD at worst site: 5.5 (0.8) (BL) to 4.1 (1.2) mm (6 months, subject level) |
 |  |  |  |  |  |  | Control |
 |  |  |  |  |  |  | BOP: 80.0 (25.0) (BL) to 47.5 (32.3) % (6 months, subject level) |
 |  |  |  |  |  |  | PD at worst site: 5.7 (0.8) (BL) to 4.9 (1.1) mm (6 months, subject level) |
 |  |  |  |  |  |  | Odds ratio of a positive treatment outcome (PD ≤ 4.0 mm and BOP ≤ 1) was 4.5:1 (test vs. control) |
 |  |  |  |  |  |  | Comparable reductions in bacterial counts |