Basheer 2017.
| Study characteristics | ||
| Methods | Study design: parallel RCT Conducted in: India |
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| Participants | Inclusion criteria: healthy patients above 20 years of age. Individuals having vertical, mesioangular, horizontal mandibular third molar impactions based on radiographic interpretation Exclusion criteria: patients with systemic disease that could influence healing, patients who do not provide consent, patients on antibiotics in the past 6 weeks or who require antibiotic prophylaxis before extraction, and patients who had acute local infection involving the impacted teeth Age: above 20 years old Number evaluated: 30 participants/30 teeth |
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| Interventions | Piezoelectric versus rotary osteotomy technique for bone removal Group I: piezoelectric osteotomy technique (frequency of 25 to 29 kHz with a microvibration of 60 to 200 mm/s was used with a boosted working mode) Group II: rotary osteotomy technique (35,000 rpm) All participants underwent surgical removal of impacted mandibular third molars under 2% lidocaine with 1:200,000 adrenaline, with inferior alveolar, lingual, and long buccal nerve blocks administered. Postoperatively, all participants received amoxicillin 500 mg 3 times a day and diclofenac sodium 50 mg 3 times a day for 3 days. Postoperative instructions were given, and the sutures were removed on the seventh day. |
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| Outcomes | Pain VAS (no pain to severe pain) Trismus (interincisal distance) Swelling Other outcomes: time taken for the procedure; patient satisfaction |
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| Notes | Descriptive analysis was done. Results are explained as mean ± standard deviation (min to max) and also as number (%): 5% was considered as level of significance with 95% confidence interval. Quantitative data were analysed using unpaired t‐test, and qualitative data were analysed using Fisher’s exact test. Sample size calculation: not reported |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Quote: "individuals were randomly allocated to study groups" Comment: method of randomisation was not described |
| Allocation concealment (selection bias) | Unclear risk | Comment: methods of concealment were not discussed |
| Blinding (performance bias and detection bias) patient | Unclear risk | Comment: it is unclear if the participants were blinded as they consented to the procedure |
| Blinding (performance bias and detection bias) assessor | Unclear risk | Comment: blinding is not mentioned |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | There were no reported dropouts. |
| Selective reporting (reporting bias) | Low risk | All of the outcomes were reported. |
| Other bias | High risk | Quote "to standardize our results, it was conducted on 30 male individuals having their age ranging from 25 to 33 years, in order to remove the gender factor that may play a role in postoperative complications due to hormonal changes that may occur in females" Comment: this study only included males, therefore the results are limited to this study population |