Assessing Efficacy of Intravenous Acetaminophen for Perioperative Pain Control for Oocyte Retrieval
Summary
Linked Publications
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Assessing efficacy of intravenous acetaminophen for perioperative pain control for oocyte retrieval: a randomized, double-blind, placebo-controlled trial.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Post-operative Pain Score Difference 10 Mins From Pre-operative |
1.3; 1.3; 1.8 | — |
| PRIMARY Time to Discharge From the Post-operative Recovery Room |
60.1; 58.8; 57.6 | — |
| SECONDARY Procedure Length |
13.5; 13.7; 14.1 | — |
| SECONDARY Postoperative Nausea and Vomiting |
3; 4; 2 | — |
| SECONDARY Oocyte Yield |
12.6; 13.4; 11.4 | — |
| SECONDARY Rescue Medication Required |
4; 10; 8 | — |
Eligibility Criteria
Inclusion Criteria
[ ] Patient is 18 years or over, undergoing oocyte retrieval. [ ] Patient is English-speaking.
Exclusion Criteria
[ ] Allergy/hypersensitivity to acetaminophen or opiates. [ ] Any history of liver disease, history of alcohol depending, or renal impairment as reported in the electronic health record.
[ ] Any history chronic opiate use or chronic pain disorder reported in the electronic health record.
[ ] Weight less than 50kg as reported in the medical record.
Data sourced from ClinicalTrials.gov (NCT03073980) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.