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Clinical Trial Summary

The purpose of this study is to determine whether propranolol is better than oxytocin for the treatment of labor abnormalities. The endpoint is the rate of vaginal delivery experienced by women receiving prolonged oxytocin versus propranolol.


Clinical Trial Description

This trial was designed to test if propranolo can reduce the c section rate for dysfuctional labor. Due to stringent inclution and exclusion criteria and low enrollment the study was closed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00315913
Study type Interventional
Source University of California, Irvine
Contact
Status Withdrawn
Phase Phase 2
Start date January 2004
Completion date March 2008

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT02910115 - Cooling the Uterus in C-section After Dysfunctional Labor N/A