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. 2021 Jun 14;2021(6):CD012978. doi: 10.1002/14651858.CD012978.pub2

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
Participants Inclusion criteria
  1. Elective periodontal flap and osseous recontouring of at least 3 teeth

  2. Aged > 18 years old

  3. Co‐operative

  4. Good health


Exclusion criteria
  1. Uncontrolled systemic disease

  2. Drug abuse

  3. Contraindication to NSAIDs

  4. Pregnancy and lactation

  5. Sedatives

  6. Antidepressants

  7. Analgesic use

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
Outcomes
  1. Postoperative pain (1‐4 ordinal scale every hour until 8 hours)

  2. Patient satisfaction (1‐5 scale at 8 hours)

  3. Time to analgesic request (hours)

  4. Adverse events (nonspecific during follow‐up)

Notes Funding: not reported
Declarations of interest: not reported
Authors contacted: no
Other: unable to include pain and patient satisfaction due to ordinal scales
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..."