Bhati 2017.
Study characteristics | ||
Methods | Study design: split‐mouth RCT Conducted in: India |
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Participants | Inclusion criteria: patients requiring bilateral surgical removal of impacted mandibular third molars and willing to take part in the study Exclusion criteria:
Age: 27.43 ± 5.27 years Number evaluated: 30 participants/60 teeth |
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Interventions | Piezoelectric versus rotary osteotomy technique for bone removal Test group: piezosurgery Control group: conventional rotary hand‐piece (35,000 rpm) Lidocaine 2% with 1:200,000 adrenaline was used for inferior alveolar nerve block along with long buccal nerve block and lingual nerve block. All participants routinely received postoperative dose of oral antibiotics in the form of capsule ampicillin 250 mg plus cloxacillin 250 mg and tablet metronidazole 400 mg 3 times daily for 5 days, and analgesics in a combination of tablet ibuprofen 400 mg and paracetamol 325 mg 3 times daily for 3 days. Participants were recalled on the first, third, and seventh postoperative days for follow‐up. |
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Outcomes | Pain VAS (0 to 10) Swelling (this was achieved using a 3‐0 silk suture to measure the distance between the angle of lower jaw (G), and each of 4 facial reference point‐linear distances to tragus, lateral canthus, alar, and pogonion were recorded) Trismus (interincisal distances) Paraesthesia: evaluated by light touch (cotton wisp) and 2‐point discrimination Dry socket (Blum criteria) |
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Notes | Sample size calculation: not reported | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Comment: method of randomisation unclear |
Allocation concealment (selection bias) | Unclear risk | Comment: concealment methods not described |
Blinding (performance bias and detection bias) patient | Unclear risk | Comment: participants signed an informed consent agreement, but details discussed are unclear |
Blinding (performance bias and detection bias) assessor | Unclear risk | Comment: unclear who carried out outcome measurements |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Comment: no dropouts mentioned |
Selective reporting (reporting bias) | Low risk | Comment: all planned outcomes reported |
Other bias | Unclear risk | Comment: split‐mouth study. No mention of when the extraction on the contralateral side took place. No analysis of any carry‐over effect |