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Clinical Trial Summary

Adding TAP block with Bupivacaine may decrease the use of PCA bolus use after caesarean section for pain relief.


Clinical Trial Description

Participants in the study will be randomized to TAP block with 0.5% or 0.25% bupivacaine or with placebo (normal saline). The number of PCA bolus used within 24 hours post cesarean section will be compared between the groups. ;


Study Design


Related Conditions & MeSH terms

  • Obstetrical Complications From Sedation During Parturition

NCT number NCT01986049
Study type Interventional
Source New York Presbyterian Brooklyn Methodist Hospital
Contact
Status Withdrawn
Phase Phase 3
Start date February 2013
Completion date August 2013