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NCT02575677 Clinical Trial

Oxycodone in Treatment of Early Labour Pain Efficacy and Safety

Labor Pain Clinical Trial

— oksisynnytys  

Official title:
Oxycodone in Treatment of Early Labour Pain Efficacy and Safety

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02575677
Other study ID # KUH26062012
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 2012
Est. completion date December 2023

Study information
Verified date March 2023
Source Kuopio University Hospital
Contact Merja Kokki, PhD
Phone +358-44-7174764
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Oxycodone is used to treat early labour pain instead of meperidine. However, the efficacy and effects of oxycodone to the newborn has not been studied. In the present study, patient who has received oxycodone is asked about pain relief and after labour single venous blood sample from the parturient and umbilical cord are taken for the analysis of oxycodone.

Recruitment information / eligibility
Status Recruiting
Enrollment 90
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Oxycodone for pain relief - age 18 years or more - given informed consent Exclusion Criteria: - no oxycodone - age less than 18 years - no informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• oxycodone
oxycodone 0,1/kg up to 10 mg sc.

Locations
Country Name City State
Finland Kuopio University Hospital Kuopio Northern Savo

Sponsors (2)
Lead Sponsor Collaborator
Kuopio University Hospital Admescope Ltd

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain measured with numerical rating scale Pain measured with numerical rating scale 0-10 (0=no pain, 10 = worst pain) from the time of oxycodone administration up to the birth of newborn, maximum of 48 hours
See also
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