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Preemptive Acetaminophen for Postoperative Pain Control Following Minimally Invasive Hysterectomy

Post Operative Pain Clinical Trial

Official title:
Preemptive Acetaminophen for Postoperative Pain Control Following Minimally Invasive Hysterectomy: a Randomized Control Trial

Clinical Trial Summary

This study is investigating whether administration of acetaminophen the day before surgery improves post operative pain following minimally invasive hysterectomy. Patients will receive either acetaminophen or placebo to take twice per day the day prior to their scheduled surgery. The morning of surgery all participants will receive oral acetaminophen at least 30 minutes prior to surgery. The investigators will examine whether there is a difference in post operative pain between the two groups.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04360135
Study type Interventional
Source Montefiore Medical Center
Contact
Status Withdrawn
Phase Phase 2/Phase 3
Start date May 6, 2020
Completion date March 8, 2021
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