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Trial · NCT03348683

Results by group24

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Time From Beginning of Induction to DeliveryPropranolol13.8Standard Deviation 5.4hours
Time From Beginning of Induction to DeliveryPlacebo14.3Standard Deviation 5.3hours
Number of Participants With Various Mode of DeliveryPropranololSpontaneous vaginal delivery64Participants
Number of Participants With Various Mode of DeliveryPlaceboSpontaneous vaginal delivery61Participants
Number of Participants With Various Mode of DeliveryPropranololVacuum assisted vaginal delivery3Participants
Number of Participants With Various Mode of DeliveryPlaceboVacuum assisted vaginal delivery10Participants
Number of Participants With Various Mode of DeliveryPropranololForceps assisted vaginal delivery8Participants
Number of Participants With Various Mode of DeliveryPlaceboForceps assisted vaginal delivery8Participants
Number of Participants With Various Mode of DeliveryPropranololCesarean section46Participants
Number of Participants With Various Mode of DeliveryPlaceboCesarean section40Participants
Duration of LatentPropranolol11.0Standard Deviation 5.0hours
Duration of LatentPlacebo11.2Standard Deviation 4.5hours
Number of Participants With Maternal Morbidity Composite Score = 1Propranolol35Participants
Number of Participants With Maternal Morbidity Composite Score = 1Placebo49Participants
Number of Participants With Postpartum HemorrhagePropranolol15Participants
Number of Participants With Postpartum HemorrhagePlacebo26Participants
Number of Fetus With Heart Rate DecelerationsPropranolol15Participants
Number of Fetus With Heart Rate DecelerationsPlacebo13Participants
Number of Fetus With Fetal BradycardiaPropranolol1Participants
Number of Fetus With Fetal BradycardiaPlacebo0Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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