Pozos‐Guillen 2007.
Methods | Study design: parallel‐group randomized controlled trial Sample size: 60 Country: Mexico Setting: secondary care hospital Dates conducted: not reported Postoperative opioid used and delivery: N/A Pain score collection: in clinic‐submitted pain evaluations Concurrent postoperative analgesics: dexamethasone 4 mg intramuscular before procedure, paracetamol 500 mg to 1000 mg or ketorolac 10 mg (or intramuscular 30 mg) depending on pain |
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Participants |
Inclusion criteria
Exclusion criteria
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Interventions |
Group A (20 participants): intramuscular tramadol 100 mg 1 hour before surgery Group B (20 participants): intramuscular tramadol 100 mg after surgery Group C (20 participants): saline placebo |
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Outcomes |
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Notes | Funding: funded by Universidad Autónoma San Luis Potosí; C0‐FAI‐04‐3.4 and C04‐FAI‐10‐10.53 Declarations of interest: not reported Authors contacted: we contacted authors for further information but received no response. Other: extracted from graphs using computer software. Unclear what errors bars represent |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Unclear details. Quote: "participants were randomized" |
Allocation concealment (selection bias) | Unclear risk | No mention |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No double‐dummy placebo |
Blinding of outcome assessment (detection bias) All outcomes | High risk | No double‐dummy placebo |
Incomplete outcome data (attrition bias) All outcomes | Low risk | It appears that all participants were followed up. |
Selective reporting (reporting bias) | High risk | Adverse events not fully reported. |
Other bias | Low risk | Similar groups and no industry funding. Quote: "demographic characteristics of the sample were similar between groups for age and gender" |