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Scheduled Cesarean Sections clinical trials

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NCT ID: NCT02143141 Terminated - Clinical trials for Postoperative Pain Management

Low Pain Prediction in Cesarean Section Patients

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The investigators are attempting to see if eliminating the amount of long acting spinal narcotic during cesarean section delivery will demonstrate pain scores with movement when evaluated 24 hours postoperatively as those that receive the standard dosage of spinal narcotic when combined with oral acetaminophen or placebo. The investigators also are evaluating if there are decreased side effects related to decreased narcotic usage.