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UnknownNCT01474304

Intravenous Acetaminophen for Craniotomy Patients

Intravenous Acetaminophen for Craniotomy Patients: A Single-blinded, Randomized Controlled Trial to Evaluate the Effect of Intravenous Acetaminophen Administered at Induction and Emergence From Craniotomy

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Swedish Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Adding intraoperative IV acetaminophen, in addition to standard analgesics, will decrease opioid requirements over the first 12 hours of postoperative recovery following craniotomy. Opioids exacerbate symptoms of nausea and vomiting. Reducing postoperative opioid use hopefully will reduce incidence of nausea and vomiting in patients after craniotomy.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophen1000 mg dose intravenous acetaminophen before craniotomy incision and a second 1000 mg dose intravenous acetaminophen 6 hours after surgery

Timeline

Start date
2011-11-01
Primary completion
2017-06-01
First posted
2011-11-18
Last updated
2016-09-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01474304. Inclusion in this directory is not an endorsement.

Intravenous Acetaminophen for Craniotomy Patients (NCT01474304) · Clinical Trials Directory