Clinical Trials Directory

Trials / Completed

CompletedNCT01016821

Oxycodone for Labor Pain - Pharmacokinetics (PK), Safety and Efficacy

The Efficacy and Safety of Intravenous Oxycodone and Plasma Oxycodone Concentrations in Labour Pain

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (estimated)
Sponsor
Kuopio University Hospital · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Childbirth is one of the most painful events that a woman is likely to experience, and thus is a major concern for most parturient. Severe pain releases stress mediators and may thus compromise fetus well-being if placental perfusion is decreased. Epidural analgesia is the golden standard for the management of severe labor pain. However, it could not always be used both due the parturient related factors and the organizational reasons.However, the knowledge on safety and efficacy of oxycodone involving mother, fetus and newborn is limited. Aim of the study is firstly, to evaluate the efficacy and safety of oxycodone in labor pain healthy parturients. Secondly, to measure parturient's blood oxycodone concentration during labour and fetal concentration from placental umbilical vein and artery right after birth.

Conditions

Interventions

TypeNameDescription
DRUGOxycodoneIntravenous, 1 mg, 5 times, in every 5 minutes, duration of drug administration 25 minutes

Timeline

Start date
2009-11-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2009-11-20
Last updated
2011-01-11

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01016821. Inclusion in this directory is not an endorsement.