Vogol 1992.
Study characteristics | ||
Methods | Study design: parallel‐group randomized controlled trial
Sample size: 36
Country: USA
Setting: secondary care hospital
Dates conducted: not reported
Postoperative opioid used and delivery: not reported Pain score collection: patient self‐scoring Concurrent postoperative analgesics: none reported |
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Participants |
Inclusion criteria
Exclusion criteria
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Interventions |
Group I‐pretreatment (19 participants): 600 mg ibuprofen 5‐10 mins before LA and placebo after suturing Group I‐post‐treatment (17 participants): placebo 5‐10 mins before LA and 600 mg ibuprofen after suturing |
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Outcomes |
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Notes | Funding: not reported Declarations of interest: not reported Authors contacted: no Other: unable to include pain and patient satisfaction due to ordinal scales |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | No mention. Quote: "Subjects were randomly distributed..." |
Allocation concealment (selection bias) | Unclear risk | No mention. Quote: "Subjects were randomly distributed..." |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Double‐dummy placebo used. Quote: "...600 mg ibuprofen immediately presurgically and placebo immediately after surgery" |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No mention |
Incomplete outcome data (attrition bias) All outcomes | High risk | Seven participants excluded. Quote: "...7 were excluded from the efficacy analysis". |
Selective reporting (reporting bias) | Unclear risk | No protocol |
Other bias | Low risk | Similar baseline characteristics. Quote: "There were no statistically significant differences..." |