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Clinical Trial Summary

Currently, the study about intervention on the induced abortion at trimester is so little. So, the investigators want to compare the safety and effectiveness of different induced labor.


Clinical Trial Description

In this study , the investigators want to compare the safety and effectiveness of different induced labor. The safety and effectiveness such as the success rate of induced labor and the gestation outcome,etc. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Caregiver, Investigator)


Related Conditions & MeSH terms

  • Labor; Forced or Induced, Affecting Fetus or Newborn

NCT number NCT02202083
Study type Interventional
Source West China Second University Hospital
Contact li zhang, Dr
Phone +8613882198624
Status Recruiting
Phase Phase 4
Start date June 2014
Completion date September 2015

See also
  Status Clinical Trial Phase
Completed NCT02273115 - Foley With Oxytocin Versus Foley no Oxytocin for Induction of Labor Phase 4
Terminated NCT02777190 - A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor Phase 4
Completed NCT02318173 - Dilapan-S/Dilasoft E-Registry in Induction of Labor N/A
Completed NCT02989571 - The Effects of Increased IV Hydration on Nulliparous Women Undergoing an Induction of Labor Early Phase 1
Recruiting NCT02210598 - Outpatient Labor Induction With the Transcervical Foley Balloon N/A
Completed NCT04271722 - Clinical Evaluation of Cervical Ripening in the Outpatient Setting N/A
Completed NCT02680314 - Is More Than One Dose of Misoprostol Needed to Expedite Vaginal Delivery in a Patient With an Unripe Cervix? Phase 2