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Clinical Trial Summary

To compare two protocols of misoprostol use for cervical ripening: 3 doses (25 ug vaginal each) or up to six doses, every six hours, until an adequate cervical condititon was achieved (BIshop score > 6). In the first group, after 3 doses, the patient was sent to the delivery room for induction with oxytocin and in case of failure, a cesarean section was indicated for this reason. In the second group, up to six doses were used in a similar fashion. Rates of success were evaluated, as well as maternal and fetal complications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03489798
Study type Interventional
Source Saint Thomas Hospital, Panama
Contact
Status Completed
Phase N/A
Start date April 5, 2018
Completion date September 15, 2018

See also
  Status Clinical Trial Phase
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Recruiting NCT03854383 - Using Isosorbide Mononitrate in Reducing Time in Induction of Labor in Post Date Women Phase 2
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