drugset / Trial / NCT02143141

Low Pain Prediction in Cesarean Section Patients

NCT02143141 ↗

Phase 4 Terminated 13 enrolled Wake Forest University Health Sciences
RandomizedParallel-groupQuadruple-blindPrevention

Summary

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.

Timeline

Start
2011-11
Primary completion
2014-08
Completion
2014-08

Outcome

Outcome not reported

Stopped: “feasibility of population needed to complete study”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Morphine Other / unclassified 150 ug Intrathecal

Indications

No indication recorded.