Trials / Completed
CompletedNCT02717637
Oxycodone in Serum After Postoperative Oral Oxycodone in Caesarean Sections Under Spinal Anesthesia
Gastrointestinal Uptake of Oxycodone After Caesarean Section in Spinal Anesthesia
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 50 (actual)
- Sponsor
- University Hospital, Akershus · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
All patients undergoing an elective caesarean section under spinal anesthesia will, according to the hospital routines, receive 10 mg oxycodone slow-release tablet when arriving at our postoperative care unit (PACU). Blood samples will be taken at 0 hour, 1 hour, 2 and 6 hours after administration in order to investigate bioavailability.
Detailed description
After written informed consent, blood samples will be taken before administration, after 1 hour, 2 hours and 6 hours. Need of rescue analgesia (morphine iv) and level of pain, as well as side effects will be registered
Conditions
Timeline
- Start date
- 2016-02-01
- Primary completion
- 2017-04-01
- Completion
- 2017-04-01
- First posted
- 2016-03-24
- Last updated
- 2018-01-12
Locations
1 site across 1 country: Norway
Source: ClinicalTrials.gov record NCT02717637. Inclusion in this directory is not an endorsement.