Clinical Trials Directory

Trials / Completed

CompletedNCT02116257

The Opioid-sparing Effect and Reduced PONV Using Propacetamol in PCA Among Patients With High Risk of PONV

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
108 (actual)
Sponsor
Yonsei University · Academic / Other
Sex
Female
Age
20 Years – 65 Years
Healthy volunteers
Accepted

Summary

While Patient-controlled analgesia (PCA) has the advantage of effectively reducing the degree of postoperative pain, it can also affect the patient's outcome by several adverse effects such as postoperative nausea and vomiting (PONV). Especially for high risk group of patients for PONV, the ideal regimen for sufficient analgesia with minimal adverse effect needs to be sought. Propacetamol is known for its effective, rapid analgesia, opioid-sparing effect, and is used widely for post operative pain management. This study aims to see the opioid-sparing effect and the degree of PONV when propacetamol is added to PCA for high risk PONV patients.

Conditions

Interventions

TypeNameDescription
DRUGPropacetamoltotal 4g of Propacetamol added to patient's PCA regimen
DRUGPCA regimen

Timeline

Start date
2013-11-01
Primary completion
2015-03-01
Completion
2015-03-01
First posted
2014-04-16
Last updated
2015-06-24

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02116257. Inclusion in this directory is not an endorsement.