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Clinical Trial Summary

The hypothesis is if administration of acetaminophen during labor will reduce the amount of neuraxial pain medication required for comfort. For the study, Acetaminophen or placebo capsules will be administered at the time of neuraxial analgesia placement and then administered every 6 hours until delivery. Overall consumption of neuraxial pain medication will be determined.


Clinical Trial Description

Acetaminophen 1000 mg or placebo capsules will be administered at the time of neuraxial analgesia placement and continued every 6 hours until delivery. Vital signs, scores for pain, nausea, itching, and sleepiness will be also obtained. Evaluation of consumption of neuraxial analgesic medication will be included in the final analysis for the differences between the 2 groups ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02181387
Study type Interventional
Source Wake Forest University Health Sciences
Contact
Status Terminated
Phase Phase 4
Start date September 5, 2013
Completion date June 2014

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