TerminatedNot Applicable

Oral Versus Intravenous Acetaminophen for Postoperative Pain Control

Stopped: It was determined that the study should not continue as the study drug, Acetaminophen, could only be mixed in a solvent that would not allow the patients to be NPO prior to procedure.

United States42 participantsStarted 2021-03-12

Plain-language summary

The investigators are going to study the difference in postoperative pain control after administration of oral versus intravenous formulation of acetaminophen

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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Inclusion criteria

✓. Provision of signed and dated informed consent form
✓. Stated willingness to comply with all study procedures and availability for the duration of the study
✓. Female, aged 18-45
✓. Ability to take oral medication and be willing to adhere to the study intervention regimen

Exclusion criteria

✕. Known clinically significant liver disfunction
✕. Known allergic reactions to components of acetaminophen such as angioedema, anaphylaxis or other
✕. Known current substance use disorder
✕. Chronic pain syndrome
✕. Weight less than 50 kg

What they're measuring

postoperative pain control

Timeframe: 24-48 hours

Trial details

NCT IDNCT04662567

SponsorNorthwell Health

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-09-05

View on ClinicalTrials.gov More Postoperative Pain trials