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Clinical Trial Summary

To evaluate the levels of morphine in a patient's blood when morphine is given into the epidural space in the form of DepoDur® either alone or following a dose of lidocaine also given in the epidural space.


Clinical Trial Description

To evaluate the levels of morphine in a patient's blood when morphine is given into the epidural space in the form of DepoDur® either alone or following a dose of lidocaine also given in the epidural space. Specifically, we are looking at pregnant women undergoing cesarean delivery who will be receiving these medications. A secondary objective is to evaluate how well DepoDur® works for pain control, as well as its safety, when it is given either alone or following a dose of epidural lidocaine. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00804609
Study type Interventional
Source Stanford University
Contact
Status Completed
Phase N/A
Start date September 2008
Completion date December 2010

See also
  Status Clinical Trial Phase
Completed NCT02813681 - Ultrasound-Guided Landmark and Epidural Site Pain N/A