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Clinical Trial Summary

Cervical ripening should be present before labor induction, which can generally be divided into two categories: pharmacological and mechanical


Clinical Trial Description

With appropriate decision and timely intervention, labor induction decreases the risk of fetal and maternal morbidity and mortality. The single balloon catheter (i.e. Foley catheter [FC]) and Cook cervical ripening balloon have been the most commonly used mechanicalwith a minimal increase in risk of cesarean section. The single balloon catheter (i.e. Foley catheter [FC]) and Cook cervical ripening balloon have been the most commonly used mechanical method. The FC applies pressure on lower uterine segment and cervix in the direction from the uterus to the vagina. The Cook cervical ripening balloon is composed of a cervicovaginal balloon and a uterine balloon. Its mechanism is similar to that of the Foley balloon, but it can apply pressure in two directions simultaneously, on both the external and internal os. Although many studies have shown that the Cook cervical ripening balloon and FC have similar efficacy and safety. They each have district advantages and disadvantages in labor induction. In addition to the cost advantage and wide avail- ability of the FC, the safety of labor induction with the FC has been proven by many studies. However, some study have shown that the FC results in a higher pain score, and consequently, higher maternal request for cesarean section and higher cervical laceration incidence compared with the Cook cervical ripening balloon. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05511727
Study type Interventional
Source Egymedicalpedia
Contact Yousry Selim, Professor
Phone +201024319294
Email elasuotyy88@gmail.com
Status Not yet recruiting
Phase N/A
Start date November 1, 2022
Completion date December 30, 2023

See also
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Active, not recruiting NCT06324279 - Cervical Sliding Sign to Predict Outcome of Induction of Labor
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Recruiting NCT03854383 - Using Isosorbide Mononitrate in Reducing Time in Induction of Labor in Post Date Women Phase 2
Completed NCT01428037 - Safety and Efficacy Study of Vaginal Misoprostol for Cervical Ripening and Induction of Labor Phase 3
Terminated NCT03752073 - Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix N/A
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Completed NCT03976037 - Buccal Versus Vaginal Misoprostol In Combination With Foley Bulb Early Phase 1