Clinical Trials Logo

Clinical Trial Summary

A double-blind placebo controlled randomized trial comparing cesarean delivery rates in women given IV propranolol versus placebo for treatment of prolonged labor.


Clinical Trial Description

A double-blind placebo controlled randomized trial comparing cesarean delivery rates in 326 women given IV propranolol (2 mg with one possible repeat dose greater than 2 hours later) versus IV placebo for treatment of prolonged labor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04299438
Study type Interventional
Source University of Pennsylvania
Contact
Status Terminated
Phase Phase 3
Start date July 14, 2020
Completion date July 15, 2022

See also
  Status Clinical Trial Phase
Completed NCT01542151 - Effects of Sleep, Fatigue, and Timing of Post-dates Inductions Among Nulliparas N/A
Completed NCT02916082 - Cervical Length Pre-induction as a Tool to Predict Vaginal Birth N/A
Recruiting NCT03607929 - HIDRATA Study: Efficacy of a Hydration Protocol in Nulliparous Women During Labor N/A
Not yet recruiting NCT04307199 - Membrane Sweeping to Prevent Post-term Pregnancy: The MILO Study N/A
Completed NCT01140971 - Foley Catheter Versus Vaginal Misoprostol for Cervical Ripening and Induction of Labor N/A
Recruiting NCT02255903 - Middle Cerebral To Umbilical Artery Doppler Ratio And Amniotic Fluid Volume Measurement In Post-date Pregnancies in King Khalid Military Central City
Not yet recruiting NCT02680093 - Birth Rate in Conservative Monitoring of Pregnancy Beyond the Date of Birth. N/A